Shape-Persistent (Pt-salphen)2 Phosphorescent Coordination Frameworks: Structural Insights and Selective Perturbations
The development of molecular frameworks derived from binuclear platinum(II) aromatic Schiff base (salphen) complexes and their supramolecular chemistry have been undertaken. A series of axially rotating (Pt‐salphen)2 luminophores, tethered in a cofacial manner by a rigid linker (xanthene, 1; dibenzo...
Saved in:
| Published in | Chemistry : a European journal Vol. 19; no. 27; pp. 8937 - 8947 |
|---|---|
| Main Authors | , , |
| Format | Journal Article |
| Language | English |
| Published |
Weinheim
WILEY-VCH Verlag
01.07.2013
WILEY‐VCH Verlag Wiley Subscription Services, Inc |
| Subjects | |
| Online Access | Get full text |
Cover
Loading…
| Abstract | The development of molecular frameworks derived from binuclear platinum(II) aromatic Schiff base (salphen) complexes and their supramolecular chemistry have been undertaken. A series of axially rotating (Pt‐salphen)2 luminophores, tethered in a cofacial manner by a rigid linker (xanthene, 1; dibenzofuran, 2; biphenylene, 3), was synthesized in which the O(salphen) groups are potentially amenable for guest‐binding. The molecular structures of 1 and 3 have been determined by X‐ray crystallography, revealing intra‐ and intermolecular π‐stacking interactions, as well as contrasting syn (1) and anti (3) configurations, for the (Pt‐salphen)2 moiety. All complexes are luminescent in solution at room temperature. Their photophysical and solvatochromic properties have been examined, and the emissions are assigned to mixed triplet O(p)/Pt(d)→π*(diimine) excited states. The red‐shifted fluid emissions and lower quantum yields of 1 and 3, relative to 2, are ascribed to enhanced intramolecular π‐stacking interactions. Photophysical changes and selective responses to metal ions (particularly Pb2+) have been investigated by using various spectroscopic methods and DFT calculations, and through comparative studies with control complexes. A plausible binding mechanism is proposed based on occupation of the O(salphen)‐binding cavity, which induces perturbation of intramolecular π–π interactions, and hence the self‐quenching and emission properties, of the (Pt‐salphen)2 unit.
To π or not to π? The ratiometric phosphorescent ion‐selective responses of axially rotating binuclear assemblies have been investigated by using X‐ray crystallography, DFT calculations, and various spectroscopic techniques to provide an insight into the binding mechanism (see figure). These results may carry important implications for stimuli‐responsive luminescent host complexes that engage in intramolecular interactions. |
|---|---|
| AbstractList | The development of molecular frameworks derived from binuclear platinum(II) aromatic Schiff base (salphen) complexes and their supramolecular chemistry have been undertaken. A series of axially rotating (Pt‐salphen)
2
luminophores, tethered in a cofacial manner by a rigid linker (xanthene,
1
; dibenzofuran,
2
; biphenylene,
3
), was synthesized in which the O(salphen) groups are potentially amenable for guest‐binding. The molecular structures of
1
and
3
have been determined by X‐ray crystallography, revealing intra‐ and intermolecular π‐stacking interactions, as well as contrasting
syn
(
1
) and
anti
(
3
) configurations, for the (Pt‐salphen)
2
moiety. All complexes are luminescent in solution at room temperature. Their photophysical and solvatochromic properties have been examined, and the emissions are assigned to mixed triplet O(p)/Pt(d)→π*(diimine) excited states. The red‐shifted fluid emissions and lower quantum yields of
1
and
3
, relative to
2
, are ascribed to enhanced intramolecular π‐stacking interactions. Photophysical changes and selective responses to metal ions (particularly Pb
2+
) have been investigated by using various spectroscopic methods and DFT calculations, and through comparative studies with control complexes. A plausible binding mechanism is proposed based on occupation of the O(salphen)‐binding cavity, which induces perturbation of intramolecular π–π interactions, and hence the self‐quenching and emission properties, of the (Pt‐salphen)
2
unit. The development of molecular frameworks derived from binuclear platinum(II) aromatic Schiff base (salphen) complexes and their supramolecular chemistry have been undertaken. A series of axially rotating (Pt‐salphen)2 luminophores, tethered in a cofacial manner by a rigid linker (xanthene, 1; dibenzofuran, 2; biphenylene, 3), was synthesized in which the O(salphen) groups are potentially amenable for guest‐binding. The molecular structures of 1 and 3 have been determined by X‐ray crystallography, revealing intra‐ and intermolecular π‐stacking interactions, as well as contrasting syn (1) and anti (3) configurations, for the (Pt‐salphen)2 moiety. All complexes are luminescent in solution at room temperature. Their photophysical and solvatochromic properties have been examined, and the emissions are assigned to mixed triplet O(p)/Pt(d)→π*(diimine) excited states. The red‐shifted fluid emissions and lower quantum yields of 1 and 3, relative to 2, are ascribed to enhanced intramolecular π‐stacking interactions. Photophysical changes and selective responses to metal ions (particularly Pb2+) have been investigated by using various spectroscopic methods and DFT calculations, and through comparative studies with control complexes. A plausible binding mechanism is proposed based on occupation of the O(salphen)‐binding cavity, which induces perturbation of intramolecular π–π interactions, and hence the self‐quenching and emission properties, of the (Pt‐salphen)2 unit. To π or not to π? The ratiometric phosphorescent ion‐selective responses of axially rotating binuclear assemblies have been investigated by using X‐ray crystallography, DFT calculations, and various spectroscopic techniques to provide an insight into the binding mechanism (see figure). These results may carry important implications for stimuli‐responsive luminescent host complexes that engage in intramolecular interactions. The development of molecular frameworks derived from binuclear platinum(II) aromatic Schiff base (salphen) complexes and their supramolecular chemistry have been undertaken. A series of axially rotating (Pt-salphen)2 luminophores, tethered in a cofacial manner by a rigid linker (xanthene, 1; dibenzofuran, 2; biphenylene, 3), was synthesized in which the O(salphen) groups are potentially amenable for guest-binding. The molecular structures of 1 and 3 have been determined by X-ray crystallography, revealing intra- and intermolecular π-stacking interactions, as well as contrasting syn (1) and anti (3) configurations, for the (Pt-salphen)2 moiety. All complexes are luminescent in solution at room temperature. Their photophysical and solvatochromic properties have been examined, and the emissions are assigned to mixed triplet O(p)/Pt(d)[arrow right]π*(diimine) excited states. The red-shifted fluid emissions and lower quantum yields of 1 and 3, relative to 2, are ascribed to enhanced intramolecular π-stacking interactions. Photophysical changes and selective responses to metal ions (particularly Pb2+) have been investigated by using various spectroscopic methods and DFT calculations, and through comparative studies with control complexes. A plausible binding mechanism is proposed based on occupation of the O(salphen)-binding cavity, which induces perturbation of intramolecular π-π interactions, and hence the self-quenching and emission properties, of the (Pt-salphen)2 unit. [PUBLICATION ABSTRACT] The development of molecular frameworks derived from binuclear platinum(II) aromatic Schiff base (salphen) complexes and their supramolecular chemistry have been undertaken. A series of axially rotating (Pt-salphen)2 luminophores, tethered in a cofacial manner by a rigid linker (xanthene, 1; dibenzofuran, 2; biphenylene, 3), was synthesized in which the O(salphen) groups are potentially amenable for guest-binding. The molecular structures of 1 and 3 have been determined by X-ray crystallography, revealing intra- and intermolecular π-stacking interactions, as well as contrasting syn (1) and anti (3) configurations, for the (Pt-salphen)2 moiety. All complexes are luminescent in solution at room temperature. Their photophysical and solvatochromic properties have been examined, and the emissions are assigned to mixed triplet O(p)/Pt(d)→π*(diimine) excited states. The red-shifted fluid emissions and lower quantum yields of 1 and 3, relative to 2, are ascribed to enhanced intramolecular π-stacking interactions. Photophysical changes and selective responses to metal ions (particularly Pb(2+)) have been investigated by using various spectroscopic methods and DFT calculations, and through comparative studies with control complexes. A plausible binding mechanism is proposed based on occupation of the O(salphen)-binding cavity, which induces perturbation of intramolecular π-π interactions, and hence the self-quenching and emission properties, of the (Pt-salphen)2 unit.The development of molecular frameworks derived from binuclear platinum(II) aromatic Schiff base (salphen) complexes and their supramolecular chemistry have been undertaken. A series of axially rotating (Pt-salphen)2 luminophores, tethered in a cofacial manner by a rigid linker (xanthene, 1; dibenzofuran, 2; biphenylene, 3), was synthesized in which the O(salphen) groups are potentially amenable for guest-binding. The molecular structures of 1 and 3 have been determined by X-ray crystallography, revealing intra- and intermolecular π-stacking interactions, as well as contrasting syn (1) and anti (3) configurations, for the (Pt-salphen)2 moiety. All complexes are luminescent in solution at room temperature. Their photophysical and solvatochromic properties have been examined, and the emissions are assigned to mixed triplet O(p)/Pt(d)→π*(diimine) excited states. The red-shifted fluid emissions and lower quantum yields of 1 and 3, relative to 2, are ascribed to enhanced intramolecular π-stacking interactions. Photophysical changes and selective responses to metal ions (particularly Pb(2+)) have been investigated by using various spectroscopic methods and DFT calculations, and through comparative studies with control complexes. A plausible binding mechanism is proposed based on occupation of the O(salphen)-binding cavity, which induces perturbation of intramolecular π-π interactions, and hence the self-quenching and emission properties, of the (Pt-salphen)2 unit. The development of molecular frameworks derived from binuclear platinum(II) aromatic Schiff base (salphen) complexes and their supramolecular chemistry have been undertaken. A series of axially rotating (Pt-salphen)2 luminophores, tethered in a cofacial manner by a rigid linker (xanthene, 1; dibenzofuran, 2; biphenylene, 3), was synthesized in which the O(salphen) groups are potentially amenable for guest-binding. The molecular structures of 1 and 3 have been determined by X-ray crystallography, revealing intra- and intermolecular π-stacking interactions, as well as contrasting syn (1) and anti (3) configurations, for the (Pt-salphen)2 moiety. All complexes are luminescent in solution at room temperature. Their photophysical and solvatochromic properties have been examined, and the emissions are assigned to mixed triplet O(p)/Pt(d)→π*(diimine) excited states. The red-shifted fluid emissions and lower quantum yields of 1 and 3, relative to 2, are ascribed to enhanced intramolecular π-stacking interactions. Photophysical changes and selective responses to metal ions (particularly Pb(2+)) have been investigated by using various spectroscopic methods and DFT calculations, and through comparative studies with control complexes. A plausible binding mechanism is proposed based on occupation of the O(salphen)-binding cavity, which induces perturbation of intramolecular π-π interactions, and hence the self-quenching and emission properties, of the (Pt-salphen)2 unit. |
| Author | Guo, Zhengqing Yiu, Shek-Man Chan, Michael C. W. |
| Author_xml | – sequence: 1 givenname: Zhengqing surname: Guo fullname: Guo, Zhengqing organization: Department of Biology and Chemistry, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong (P.R. China) – sequence: 2 givenname: Shek-Man surname: Yiu fullname: Yiu, Shek-Man organization: Department of Biology and Chemistry, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong (P.R. China) – sequence: 3 givenname: Michael C. W. surname: Chan fullname: Chan, Michael C. W. email: mcwchan@cityu.edu.hk organization: Department of Biology and Chemistry, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong (P.R. China) |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23682037$$D View this record in MEDLINE/PubMed |
| BookMark | eNqFkctv1DAQhy1URLeFK0cUiUs5ZPEjiWNuVdSXKGVhQSAulpNMiNvEDrbTx3_fpNtWqBLiZEvzfeMZ_3bQlrEGEHpN8JJgTN9XLfRLignDOKHkGVqQlJKY8SzdQgssEh5nKRPbaMf7c4yxyBh7gbYpy3KKGV-gy3WrBohX4Lz2AUyI9lYh9qobWjDvaLRqrR9a68BXc7Gw1tXaqKCtiQ6d6uHKugv_IVoHN1ZhdKqLTozXv9vgI2XqaA0dVEFfQjQ9MdXLO9W_RM8b1Xl4dX_uou-HB9-K4_j089FJsX8aVwnnJCYpCJ4LKljCckFyKJssE6VISJURTkpcQ12nGMrpxpNGNEkFjPCSYeBl3qRsF-1t-g7O_hnBB9nraZOuUwbs6CVhnFCO0xxP6Nsn6LkdnZmmmylMsgRzOlFv7qmx7KGWg9O9cjfy4UcnINkAlbPeO2hkpcPd0sEp3UmC5RycnIOTj8FN2vKJ9tD5n4LYCFe6g5v_0LI4Pvj0txtv3Dny60dXuQuZccZT-ePsSK4-sq-_fhZf5Bm7BbXzuvU |
| CODEN | CEUJED |
| CitedBy_id | crossref_primary_10_1039_C5CC08794E crossref_primary_10_1002_ejic_202001117 crossref_primary_10_1016_j_ccr_2018_04_003 crossref_primary_10_1002_ejic_201600231 crossref_primary_10_1039_c4dt00591k crossref_primary_10_1039_C6CE02073A crossref_primary_10_1021_acs_inorgchem_5b02231 crossref_primary_10_1002_anie_202115712 crossref_primary_10_1055_s_0040_1708501 crossref_primary_10_1016_j_ica_2017_01_031 crossref_primary_10_1002_chem_201703675 crossref_primary_10_1016_j_poly_2016_04_022 crossref_primary_10_1021_acs_macromol_7b01269 crossref_primary_10_1039_C3DT52034J crossref_primary_10_1021_acs_cgd_6b00347 crossref_primary_10_1039_C7SC04537A crossref_primary_10_3390_molecules23050990 crossref_primary_10_1039_C5CC06253E crossref_primary_10_1021_acs_chemrev_5b00074 crossref_primary_10_1039_C9DT02595B crossref_primary_10_1039_D4NJ03357D crossref_primary_10_1002_ange_202115712 crossref_primary_10_1002_chem_201404064 crossref_primary_10_1021_acs_chemmater_8b00614 crossref_primary_10_1021_ic5000815 crossref_primary_10_1016_j_ejmech_2016_08_053 crossref_primary_10_1039_D3TC03432A crossref_primary_10_1039_c3cc47150k crossref_primary_10_1039_C4DT03230F crossref_primary_10_1002_ejic_201402459 crossref_primary_10_1039_C9TC01585J crossref_primary_10_1021_ic400692x crossref_primary_10_1021_jacs_4c17146 crossref_primary_10_1039_c3dt53397b crossref_primary_10_1021_acs_inorgchem_2c03480 |
| Cites_doi | 10.1039/b517944k 10.1021/ja961065y 10.1021/ic00023a032 10.1002/chem.200306045 10.1021/ja804076q 10.1002/ange.201002776 10.1039/b515558d 10.1039/b402318h 10.1021/ja070358w 10.1021/ja951345y 10.1021/ja900257k 10.1039/b100604p 10.1021/ja0646702 10.1039/b925560e 10.1002/ange.19941061505 10.1021/ja058731s 10.1002/chem.200801149 10.1021/ja042807n 10.1021/ic901937p 10.1039/c0sc00220h 10.1039/c2cy20171b 10.1021/ja028910z 10.1002/chem.201200335 10.1021/ja910886g 10.1039/C0CC04493H 10.1021/ja910419h 10.1021/ja7113618 10.1021/ar9000108 10.1002/chem.200902031 10.1021/ja043682p 10.1021/ja00053a014 10.1002/chem.200900238 10.1038/nchem.900 10.1021/ja039727o 10.1021/ja031600b 10.1021/ol200532t 10.1002/ange.200500058 10.1021/ic00122a015 10.1021/ja00180a038 10.1021/ma201078m 10.1021/ja111583e 10.1016/j.poly.2007.06.029 10.1002/ejic.200200665 10.1021/ic200785g 10.1039/b618833h 10.1002/anie.198800891 10.1002/anie.200704347 10.1002/chem.200901943 10.1021/ja982683c 10.1002/anie.199510191 10.1002/chem.200902183 10.1002/anie.199415371 10.1021/ja106484t 10.1002/ange.200704347 10.1002/ange.19881000110 10.1021/ja017309i 10.1021/ar0200448 10.1002/marc.201000266 10.1002/ange.19951070914 10.1021/ja037836x 10.1021/ja00483a063 10.1002/chem.200902712 10.1039/b900030e 10.1002/anie.200460932 10.1002/(SICI)1521-3765(19991001)5:10<2845::AID-CHEM2845>3.0.CO;2-G 10.1021/ic00129a003 10.1021/ja005701a 10.1039/b904665h 10.1002/ange.200460932 10.1021/ja047955s 10.1021/ja202136y 10.1002/anie.201004957 10.1021/ol8001317 10.1039/c1dt11001b 10.1039/C1CS15170C 10.1039/b922212j 10.1002/ange.201004957 10.1021/ic990189j 10.1021/ja910724x 10.1021/ja00004a027 10.1039/b603985e 10.1002/anie.200500058 10.1021/ja042849b 10.1021/om0009839 10.1039/b006375o 10.1021/ja8051552 10.1021/ar900118t 10.1021/ja106050s 10.1021/ic990238s 10.1021/ic8006876 10.1002/ange.200352395 10.1002/chem.200902328 10.1021/om1007488 10.1021/ja0687522 10.1002/chem.200390143 10.1039/b909645k 10.1021/om700481f 10.1002/anie.200352395 10.1039/b719548f 10.1021/ja2039369 10.1021/ja017298t 10.1021/ja306473x 10.1039/b609880k 10.1021/ja202138m 10.1002/chem.200902188 10.1039/b903963e 10.1039/c2dt30444a 10.1002/anie.201002776 |
| ContentType | Journal Article |
| Copyright | Copyright © 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim |
| Copyright_xml | – notice: Copyright © 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim – notice: Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. – notice: Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim |
| DBID | BSCLL AAYXX CITATION NPM 7SR 8BQ 8FD JG9 K9. 7X8 |
| DOI | 10.1002/chem.201300421 |
| DatabaseName | Istex CrossRef PubMed Engineered Materials Abstracts METADEX Technology Research Database Materials Research Database ProQuest Health & Medical Complete (Alumni) MEDLINE - Academic |
| DatabaseTitle | CrossRef PubMed Materials Research Database ProQuest Health & Medical Complete (Alumni) Engineered Materials Abstracts Technology Research Database METADEX MEDLINE - Academic |
| DatabaseTitleList | CrossRef Materials Research Database MEDLINE - Academic PubMed |
| Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
| DeliveryMethod | fulltext_linktorsrc |
| Discipline | Chemistry |
| EISSN | 1521-3765 |
| EndPage | 8947 |
| ExternalDocumentID | 3001229561 23682037 10_1002_chem_201300421 CHEM201300421 ark_67375_WNG_PK3RZXCQ_N |
| Genre | article Journal Article |
| GrantInformation_xml | – fundername: Research Grants Council of the Hong Kong SAR, China funderid: 100408; 100212 – fundername: University Grants Committee of the Hong Kong SAR, China |
| GroupedDBID | --- -DZ -~X .3N .GA .Y3 05W 0R~ 10A 1L6 1OB 1OC 1ZS 29B 33P 3SF 3WU 4.4 4ZD 50Y 50Z 51W 51X 52M 52N 52O 52P 52S 52T 52U 52W 52X 53G 5GY 5VS 66C 6J9 702 77Q 7PT 8-0 8-1 8-3 8-4 8-5 8UM 930 A03 AAESR AAEVG AAHHS AANLZ AAONW AASGY AAXRX AAZKR ABCQN ABCUV ABDBF ABIJN ABJNI ABLJU ABPVW ACAHQ ACBWZ ACCFJ ACCZN ACGFS ACIWK ACNCT ACPOU ACXBN ACXQS ADBBV ADEOM ADIZJ ADKYN ADMGS ADOZA ADXAS ADZMN ADZOD AEEZP AEGXH AEIGN AEIMD AEQDE AEUQT AEUYR AFBPY AFFPM AFGKR AFPWT AFRAH AFZJQ AHBTC AHMBA AITYG AIURR AIWBW AJBDE AJXKR ALAGY ALMA_UNASSIGNED_HOLDINGS AMBMR AMYDB ASPBG ATUGU AUFTA AVWKF AZBYB AZFZN AZVAB BAFTC BDRZF BFHJK BHBCM BMNLL BMXJE BNHUX BROTX BRXPI BSCLL BY8 CS3 D-E D-F DCZOG DPXWK DR2 DRFUL DRSTM EBD EBS EJD F00 F01 F04 F5P G-S G.N GNP GODZA H.T H.X HBH HGLYW HHY HHZ HZ~ IX1 J0M JPC KQQ LATKE LAW LC2 LC3 LEEKS LH4 LITHE LOXES LP6 LP7 LUTES LW6 LYRES MEWTI MK4 MRFUL MRSTM MSFUL MSSTM MXFUL MXSTM N04 N05 N9A NF~ NNB O66 O9- OIG P2W P2X P4D PQQKQ Q.N Q11 QB0 QRW R.K RGC RNS ROL RWI RX1 RYL SUPJJ TN5 TWZ UB1 UPT V2E V8K W8V W99 WBFHL WBKPD WH7 WIB WIH WIK WJL WOHZO WQJ WRC WXSBR WYISQ XG1 XPP XV2 YZZ ZZTAW ~IA ~WT AAHQN AAMNL AANHP AAYCA ACRPL ACUHS ACYXJ ADNMO AFWVQ ALVPJ .GJ 186 31~ 6TJ 9M8 AAYXX ABEML ACSCC AETEA AEYWJ AGCDD AGHNM AGQPQ AGYGG AI. BZBRT CITATION FEDTE HF~ HVGLF H~9 MVM PALCI RIWAO RJQFR SAMSI UQL VH1 Y6R ZGI NPM 7SR 8BQ 8FD JG9 K9. 7X8 |
| ID | FETCH-LOGICAL-c4771-15e9789293438918ebf669b941c6171b0dedd50ebb0d74f9f4ce317b30e7b8f53 |
| IEDL.DBID | DR2 |
| ISSN | 0947-6539 1521-3765 |
| IngestDate | Fri Jul 11 16:20:56 EDT 2025 Fri Jul 25 10:28:39 EDT 2025 Mon Jul 21 06:04:55 EDT 2025 Thu Apr 24 23:01:17 EDT 2025 Tue Jul 01 03:34:36 EDT 2025 Wed Jan 22 16:27:19 EST 2025 Wed Oct 30 09:53:37 EDT 2024 |
| IsPeerReviewed | true |
| IsScholarly | true |
| Issue | 27 |
| Language | English |
| License | http://onlinelibrary.wiley.com/termsAndConditions#vor Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
| LinkModel | DirectLink |
| MergedId | FETCHMERGED-LOGICAL-c4771-15e9789293438918ebf669b941c6171b0dedd50ebb0d74f9f4ce317b30e7b8f53 |
| Notes | Research Grants Council of the Hong Kong SAR, China - No. 100408; No. 100212 istex:94FB8A40E0BDE4A0BB032DB70A6B3052619ACDCC ArticleID:CHEM201300421 ark:/67375/WNG-PK3RZXCQ-N University Grants Committee of the Hong Kong SAR, China ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
| PMID | 23682037 |
| PQID | 1370164072 |
| PQPubID | 986340 |
| PageCount | 11 |
| ParticipantIDs | proquest_miscellaneous_1371270580 proquest_journals_1370164072 pubmed_primary_23682037 crossref_citationtrail_10_1002_chem_201300421 crossref_primary_10_1002_chem_201300421 wiley_primary_10_1002_chem_201300421_CHEM201300421 istex_primary_ark_67375_WNG_PK3RZXCQ_N |
| ProviderPackageCode | CITATION AAYXX |
| PublicationCentury | 2000 |
| PublicationDate | July 1, 2013 |
| PublicationDateYYYYMMDD | 2013-07-01 |
| PublicationDate_xml | – month: 07 year: 2013 text: July 1, 2013 day: 01 |
| PublicationDecade | 2010 |
| PublicationPlace | Weinheim |
| PublicationPlace_xml | – name: Weinheim – name: Germany |
| PublicationSubtitle | A European Journal |
| PublicationTitle | Chemistry : a European journal |
| PublicationTitleAlternate | Chem. Eur. J |
| PublicationYear | 2013 |
| Publisher | WILEY-VCH Verlag WILEY‐VCH Verlag Wiley Subscription Services, Inc |
| Publisher_xml | – name: WILEY-VCH Verlag – name: WILEY‐VCH Verlag – name: Wiley Subscription Services, Inc |
| References | Angew. Chem. Int. Ed. 2010, 49, 6430-6433 B. A. Rodriguez, M. Delferro, T. J. Marks, J. Am. Chem. Soc. 2009, 131, 5902-5919 A. C. W. Leung, J. K.-H. Hui, J. H. Chong, M. J. MacLachlan, Dalton Trans. 2009, 5199-5210 A. J. Gallant, M. J. MacLachlan, Angew. Chem. 2003, 115, 5465-5468 F. Cozzi, F. Ponzini, R. Annunziata, M. Cinquini, J. S. Siegel, Angew. Chem. 1995, 107, 1092-1094 M. Barboiu, L. Prodi, M. Montalti, N. Zaccheroni, N. Kyritsakas, J.-M. Lehn, Chem. Eur. J. 2004, 10, 2953-2959 J. H. Chong, S. Jooya Ardakani, K. J. Smith, M. J. MacLachlan, Chem. Eur. J. 2009, 15, 11824-11828 Z. Guo, W.-L. Tong, M. C. W. Chan, Chem. Commun. 2009, 6189-6191. C.-M. Che, C.-C. Kwok, S.-W. Lai, A. F. Rausch, W. J. Finkenzeller, N. Zhu, H. Yersin, Chem. Eur. J. 2010, 16, 233-247. M. D. Pluth, R. G. Bergman, K. N. Raymond, Acc. Chem. Res. 2009, 42, 1650-1659. M. Taherimehr, A. Decortes, S. M. Al-Amsyar, W. Lueangchaichaweng, C. J. Whiteoak, E. C. Escudero-Adán, A. W. Kleij, P. P. Pescarmona, Catal. Sci. Technol. 2012, 2, 2231-2237. S. Dutta, D.-K. Bučar, L. R. MacGillivray, Org. Lett. 2011, 13, 2260-2262 N. Komiya, T. Muraoka, M. Iida, M. Miyanaga, K. Takahashi, T. Naota, J. Am. Chem. Soc. 2011, 133, 16054-16061. P. C. B. Widger, S. M. Ahmed, G. W. Coates, Macromolecules 2011, 44, 5666-5670. A. L. Balch, V. J. Catalano, M. A. Chatfield, J. K. Nagle, M. M. Olmstead, P. E. Reedy, Jr., J. Am. Chem. Soc. 1991, 113, 1252-1258. S. D. Cummings, R. Eisenberg, J. Am. Chem. Soc. 1996, 118, 1949-1960. C. T. L. Ma, M. J. MacLachlan, Angew. Chem. 2005, 117, 4250-4254 J. Y. Yang, D. G. Nocera, J. Am. Chem. Soc. 2007, 129, 8192-8198. A. J. Goshe, I. M. Steele, B. Bosnich, J. Am. Chem. Soc. 2003, 125, 444-451 S. Ulrich, J.-M. Lehn, Chem. Eur. J. 2009, 15, 5640-5645 Angew. Chem. Int. Ed. 2003, 42, 5307-5310 J. K.-H. Hui, M. J. MacLachlan, Chem. Commun. 2006, 2480-2482 Y. Hong, J. W. Y. Lam, B. Z. Tang, Chem. Commun. 2009, 4332-4353. W. Lu, M. C. W. Chan, K.-K. Cheung, C.-M. Che, Organometallics 2001, 20, 2477-2486. S. J. Wezenberg, G. Salassa, E. C. Escudero-Adán, J. Benet-Buchholz, A. W. Kleij, Angew. Chem. 2011, 123, 739-742 E. R. Libra, M. J. Scott, Chem. Commun. 2006, 1485-1487 W.-L. Tong, M. C. W. Chan, S.-M. Yiu, Organometallics 2010, 29, 6377-6383. J. R. Berenguer, A. Díez, J. Fernández, J. Forniés, A. García, B. Gil, E. Lalinde, M. T. Moreno, Inorg. Chem. 2008, 47, 7703-7716. J. Dömer, J. C. Slootweg, F. Hupka, K. Lammertsma, F. E. Hahn, Angew. Chem. 2010, 122, 6575-6578 P. D. Frischmann, J. Jiang, J. K.-H. Hui, J. J. Grzybowski, M. J. MacLachlan, Org. Lett. 2008, 10, 1255-1258 K.-H. Wong, M. C. W. Chan, C.-M. Che, Chem. Eur. J. 1999, 5, 2845-2849 E. Ohta, H. Sato, S. Ando, A. Kosaka, T. Fukushima, D. Hashizume, M. Yamasaki, K. Hasegawa, A. Muraoka, H. Ushiyama, K. Yamashita, T. Aida, Nat. Chem. 2011, 3, 68-73. R. G. Konsler, J. Karl, E. N. Jacobsen, J. Am. Chem. Soc. 1998, 120, 10780-10781 M. Martínez Belmonte, S. J. Wezenberg, R. M. Haak, D. Anselmo, E. C. Escudero-Adán, J. Benet-Buchholz, A. W. Kleij, Dalton Trans. 2010, 39, 4541-4550 V. J. Chebny, R. Rathore, J. Am. Chem. Soc. 2007, 129, 8458-8465 C. Wolf, S. Liu, B. C. Reinhardt, Chem. Commun. 2006, 4242-4244. J. V. Mello, N. S. Finney, J. Am. Chem. Soc. 2005, 127, 10124-10125 M.-J. Li, C.-C. Ko, G.-P. Duan, N. Zhu, V. W.-W. Yam, Organometallics 2007, 26, 6091-6098 M. Shibasaki, M. Kanai, S. Matsunaga, N. Kumagai, Acc. Chem. Res. 2009, 42, 1117-1127 H. J. Yoon, C. A. Mirkin, J. Am. Chem. Soc. 2008, 130, 11590-11591 Angew. Chem. Int. Ed. 2004, 43, 5503-5507 S. Akine, T. Taniguchi, T. Nabeshima, J. Am. Chem. Soc. 2006, 128, 15765-15774 M.-L. Ho, Y.-M. Cheng, L.-C. Wu, P.-T. Chou, G.-H. Lee, F.-C. Hsu, Y. Chi, Polyhedron 2007, 26, 4886-4892. T. J. Dunn, C. F. Ramogida, C. Simmonds, A. Paterson, E. W. Y. Wong, L. Chiang, Y. Shimazaki, T. Storr, Inorg. Chem. 2011, 50, 6746-6755 H. Yoo, J. Yang, A. Yousef, M. R. Wasielewski, D. Kim, J. Am. Chem. Soc. 2010, 132, 3939-3944 P. D. Frischmann, G. A. Facey, P. Y. Ghi, A. J. Gallant, D. L. Bryce, F. Lelj, M. J. MacLachlan, J. Am. Chem. Soc. 2010, 132, 3893-3908 C.-T. Chen, Y.-H. Lin, T.-S. Kuo, J. Am. Chem. Soc. 2008, 130, 12842-12843. E. Benaksas Schwartz, C. B. Knobler, D. J. Cram, J. Am. Chem. Soc. 1992, 114, 10775-10784 Angew. Chem. Int. Ed. Engl. 1988, 27, 89-112 J. He, J. L. Crase, S. H. Wadumethrige, K. Thakur, L. Dai, S. Zou, R. Rathore, C. S. Hartley, J. Am. Chem. Soc. 2010, 132, 13848-13857 W.-L. Tong, M. C. W. Chan, N. Zhu, S.-K. Leung, Dalton Trans. 2009, 4741-4746 S.-Y. Liu, D. G. Nocera, J. Am. Chem. Soc. 2005, 127, 5278-5279 T. J. Wadas, Q.-M. Wang, Y.-J. Kim, C. Flaschenreim, T. N. Blanton, R. Eisenberg, J. Am. Chem. Soc. 2004, 126, 16841-16849 Z. Guo, M. C. W. Chan, Chem. Eur. J. 2009, 15, 12585-12588. K. Hiratani, M. Albrecht, Chem. Soc. Rev. 2008, 37, 2413-2421 Angew. Chem. Int. Ed. Engl. 1994, 33, 1537-1554 J. S. Nowick, P. Ballester, F. Ebmeyer, J. Rebek, Jr., J. Am. Chem. Soc. 1990, 112, 8902-8906 A. W. Kleij, Chem. Eur. J. 2008, 14, 10520-10529 J. A. A. W. Elemans, S. J. Wezenberg, M. J. J. Coenen, E. C. Escudero-Adán, J. Benet-Buchholz, D. den Boer, S. Speller, A. W. Kleij, S. De Feyter, Chem. Commun. 2010, 46, 2548-2550. F. H. Zelder, J. Rebek Jr., Chem. Commun. 2006, 753-754 J. K.-H. Hui, P. D. Frischmann, C.-H. Tso, C. A. Michal, M. J. MacLachlan, Chem. Eur. J. 2010, 16, 2453-2460 W. Wu, J. Sun, S. Ji, W. Wu, J. Zhao, H. Guo, Dalton Trans. 2011, 40, 11550-11561. P. D. Frischmann, S. Guieu, R. Tabeshi, M. J. MacLachlan, J. Am. Chem. Soc. 2010, 132, 7668-7675. P. Wu, D.-L. Ma, C.-H. Leung, S.-C. Yan, N. Zhu, R. Abagyan, C.-M. Che, Chem. Eur. J. 2009, 15, 13008-13021. M. M. Elmahdy, X. Dou, M. Mondeshki, G. Floudas, H.-J. Butt, H. W. Spiess, K. Müllen, J. Am. Chem. Soc. 2008, 130, 5311-5319 S. I. Vagin, R. Reichardt, S. Klaus, B. Rieger, J. Am. Chem. Soc. 2010, 132, 14367-14369 K. Rurack, U. Resch-Genger, Chem. Soc. Rev. 2002, 31, 116-127. V. M. Miskowski, V. H. Houlding, Inorg. Chem. 1991, 30, 4446-4452 C.-M. Che, S.-C. Chan, H.-F. Xiang, M. C. W. Chan, Y. Liu, Y. Wang, Chem. Commun. 2004, 1484-1485 Y. Shen, B. P. Sullivan, Inorg. Chem. 1995, 34, 6235-6236 A. C. W. Leung, M. J. MacLachlan, J. Mater. Chem. 2007, 17, 1923-1932. W. Lu, M. C. W. Chan, N. Zhu, C.-M. Che, C. Li, Z. Hui, J. Am. Chem. Soc. 2004, 126, 7639-7651. K. E. Splan, A. M. Massari, G. A. Morris, S.-S. Sun, E. Reina, S. T. Nguyen, J. T. Hupp, Eur. J. Inorg. Chem. 2003, 2348-2351 C. H. Lee, D. K. Dogutan, D. G. Nocera, J. Am. Chem. Soc. 2011, 133, 8775-8777 H. Houjou, M. Ito, K. Araki, Inorg. Chem. 2009, 48, 10703-10707. J. P. Collman, P. S. Wagenknecht, J. E. Hutchison, Angew. Chem. 1994, 106, 1620-1639 K. Nakano, S. Hashimoto, K. Nozaki, Chem. Sci. 2010, 1, 369-373 T.-Q. Nguyen, R. Martel, P. Avouris, M. L. Bushey, L. Brus, C. Nuckolls, J. Am. Chem. Soc. 2004, 126, 5234-5242 I. Pochorovski, M.-O. Ebert, J.-P. Gisselbrecht, C. Boudon, W. B. Schweizer, F. Diederich, J. Am. Chem. Soc. 2012, 134, 14702-14705. Y.-Y. Lin, S.-C. Chan, M. C. W. Chan, Y.-J. Hou, N. Zhu, C.-M. Che, Y. Liu, Y. Wang, Chem. Eur. J. 2003, 9, 1263-1272 N. C. Gianneschi, S.-H. Cho, S. T. Nguyen, C. A. Mirkin, Angew. Chem. 2004, 116, 5619-5623 T. Nakano, T. Yade, J. Am. Chem. Soc. 2003, 125, 15474-15484 Angew. Chem. Int. Ed. Engl. 1995, 34, 1019-1020 L. Carbonaro, M. Isola, P. La Pegna, L. Senatore, F. Marchetti, Inorg. Chem. 1999, 38, 5519-5525. F.-G. Klärner, B. Kahlert, Acc. Chem. Res. 2003, 36, 919-932 J. K.-H. Hui, Z. Yu, T. Mirfakhrai, M. J. MacLachlan, Chem. Eur. J. 2009, 15, 13456-13465 G. Li, W. Yu, J. Ni, T. Liu, Y. Liu, E. Sheng, Y. Cui, Angew. Chem. 2008, 120, 1265-1269 Angew. Chem. Int. Ed. 2008, 47, 1245-1249 T. J. Dunn, L. Chiang, C. F. Ramogida, M. I. Webb, D. Savard, M. Sakaguchi, T. Ogura, Y. Shimazaki, T. Storr, Dalton Trans. 2012, 41, 7905-7914. S. M. H. Kabir, M. Hasegawa, Y. Kuwatani, M. Yoshida, H. Matsuyama, M. Iyoda, J. Chem. Soc. Perkin Trans. 1 2001, 159-165. J.-M. Lehn, Angew. Chem. 1988, 100, 91-116 S. A. McFarland, N. S. Finney, J. Am. Chem. Soc. 2001, 123, 1260-1261 M. V. Escárcega-Bobadilla, G. Salassa, M. Martínez Belmonte, E. C. Escudero-Adán, A. W. Kleij, Chem. Eur. J. 2012, 18, 6805-6810. J. Rosenthal, T. D. Luckett, J. M. Hodgkiss, D. G. Nocera, J. Am. Chem. Soc. 2006, 128, 6546-6547 Angew. Chem. Int. Ed. 2005, 44, 4178-4182 A. Rajca, A. Safronov, S. Rajca, C. R. Ross II, J. J. Stezowski, J. Am. Chem. Soc. 1996, 118, 7272-7279. Angew. Chem. Int. Ed. 2011, 50, 713-716. T. Mizuno, W.-H. Wei, L. R. Eller, J. L. Sessler, J. Am. Chem. Soc. 2002, 124, 1134-1135 S. Guieu, A. K. Crane, M. J. MacLachlan, Chem. Commun. 2011, 47, 1169-1171. C. J. Whiteoak, G. Salassa, A. W. Kleij, Chem. Soc. Rev. 2012, 41, 622-631. S.-W. Lai, M. C. W. Chan, T.-C. Cheung, S.-M. Peng, C.-M. Che, Inorg. Chem. 1999, 38, 4046-4055 J. A. Bailey, M. G. Hill, R. E. Marsh, V. M. Miskowski, W. P. Schaefer, H. B. Gray, Inorg. Chem. 1995, 34, 4591-4599 S. A. McFarland, N. S. Finney, J. Am. Chem. Soc. 2002, 124, 1178-1179 C. W. Chen, H. W. Whitlock, Jr., J. Am. Chem. Soc. 1978, 100, 4921-4922. S. Sun, W.-L. Tong, M. C. W. Chan, Macromol. Rapid Commun. 2010, 31, 1965-1969. D. K. Dogutan, R. McGuire, Jr., D. G. Nocera, J. Am. Chem. Soc. 2011, 133, 9178-9180. D. P. Iwaniuk, C. Wolf, J. Am. Chem. Soc. 2011, 133, 2414-2417. M. Cametti, M. Nissinen, A. Dalla Cort, L. Mandolini, K. Rissanen, J. Am. Chem. Soc. 2005, 127, 3831-3837 2010; 16 2004; 126 1991; 113 2009; 42 1995; 34 2010 2010; 122 49 2008; 37 2012; 18 2011; 13 2011 2011; 123 50 2009; 48 1988 1988; 100 27 2010; 1 2012; 134 2001 2010; 29 1992; 114 2003; 9 1978; 100 1995 1995; 107 34 2003; 125 2006; 128 2009; 15 2005 2005; 117 44 1998; 120 2007; 26 2007; 17 2001; 123 2004 2004; 116 43 2010; 31 2007; 129 2002; 31 2010; 39 1991; 30 2011; 40 2008; 14 2009 2003; 36 2006 2008; 10 1994 1994; 106 33 2004 2003 2009; 131 2011; 3 1999; 5 2011; 133 2001; 20 2004; 10 2012; 2 2003 2003; 115 42 2010; 46 2002; 124 1999; 38 2005; 127 2011; 50 2010; 132 2008; 47 2011; 44 2011; 47 1990; 112 2008 2008; 120 47 2008; 130 1996; 118 2012; 41 e_1_2_6_72_2 e_1_2_6_114_2 e_1_2_6_53_2 e_1_2_6_95_2 e_1_2_6_30_2 e_1_2_6_118_2 e_1_2_6_91_2 e_1_2_6_110_2 e_1_2_6_19_2 e_1_2_6_34_3 e_1_2_6_34_2 e_1_2_6_11_2 e_1_2_6_38_2 e_1_2_6_76_2 e_1_2_6_15_2 e_1_2_6_57_2 e_1_2_6_99_2 e_1_2_6_102_2 e_1_2_6_125_2 e_1_2_6_83_2 e_1_2_6_64_2 e_1_2_6_106_2 e_1_2_6_41_2 e_1_2_6_60_2 e_1_2_6_121_2 e_1_2_6_9_3 e_1_2_6_9_2 e_1_2_6_5_2 e_1_2_6_22_2 e_1_2_6_49_2 e_1_2_6_1_2 e_1_2_6_87_2 e_1_2_6_26_2 e_1_2_6_45_2 e_1_2_6_68_2 e_1_2_6_50_2 e_1_2_6_73_2 e_1_2_6_96_2 e_1_2_6_113_2 e_1_2_6_31_2 e_1_2_6_92_2 e_1_2_6_117_2 e_1_2_6_12_2 e_1_2_6_35_2 e_1_2_6_58_2 e_1_2_6_16_2 e_1_2_6_39_2 e_1_2_6_54_2 e_1_2_6_77_2 e_1_2_6_16_3 e_1_2_6_61_2 e_1_2_6_84_2 e_1_2_6_124_2 e_1_2_6_42_2 e_1_2_6_105_2 e_1_2_6_80_2 e_1_2_6_128_2 e_1_2_6_109_2 e_1_2_6_120_2 e_1_2_6_101_2 e_1_2_6_2_3 e_1_2_6_6_2 e_1_2_6_23_2 e_1_2_6_69_2 e_1_2_6_2_2 e_1_2_6_65_2 e_1_2_6_88_2 e_1_2_6_27_2 e_1_2_6_46_2 e_1_2_6_51_2 e_1_2_6_97_2 e_1_2_6_74_3 e_1_2_6_74_2 e_1_2_6_116_2 e_1_2_6_93_2 e_1_2_6_70_2 e_1_2_6_112_2 e_1_2_6_13_2 e_1_2_6_59_2 e_1_2_6_59_3 e_1_2_6_32_2 e_1_2_6_17_2 e_1_2_6_55_2 e_1_2_6_36_2 e_1_2_6_78_2 e_1_2_6_62_2 e_1_2_6_104_2 e_1_2_6_127_2 e_1_2_6_85_2 e_1_2_6_20_2 e_1_2_6_108_2 e_1_2_6_81_2 e_1_2_6_100_2 e_1_2_6_123_2 e_1_2_6_7_2 e_1_2_6_3_2 e_1_2_6_24_2 e_1_2_6_47_2 e_1_2_6_28_2 e_1_2_6_43_2 e_1_2_6_66_2 e_1_2_6_89_3 e_1_2_6_89_2 e_1_2_6_52_2 e_1_2_6_75_2 e_1_2_6_94_2 e_1_2_6_115_2 e_1_2_6_71_2 e_1_2_6_90_2 e_1_2_6_119_2 e_1_2_6_111_2 e_1_2_6_18_2 e_1_2_6_33_3 e_1_2_6_10_2 e_1_2_6_33_2 e_1_2_6_14_2 e_1_2_6_37_2 e_1_2_6_56_2 e_1_2_6_79_2 e_1_2_6_98_2 e_1_2_6_14_3 e_1_2_6_103_2 e_1_2_6_63_2 e_1_2_6_86_2 e_1_2_6_126_2 e_1_2_6_107_2 e_1_2_6_40_2 e_1_2_6_82_2 e_1_2_6_122_2 e_1_2_6_8_2 e_1_2_6_29_2 e_1_2_6_4_2 e_1_2_6_48_2 e_1_2_6_21_2 e_1_2_6_44_2 e_1_2_6_67_2 e_1_2_6_25_2 |
| References_xml | – reference: J. A. Bailey, M. G. Hill, R. E. Marsh, V. M. Miskowski, W. P. Schaefer, H. B. Gray, Inorg. Chem. 1995, 34, 4591-4599; – reference: C. Wolf, S. Liu, B. C. Reinhardt, Chem. Commun. 2006, 4242-4244. – reference: S. A. McFarland, N. S. Finney, J. Am. Chem. Soc. 2001, 123, 1260-1261; – reference: J. P. Collman, P. S. Wagenknecht, J. E. Hutchison, Angew. Chem. 1994, 106, 1620-1639; – reference: J. He, J. L. Crase, S. H. Wadumethrige, K. Thakur, L. Dai, S. Zou, R. Rathore, C. S. Hartley, J. Am. Chem. Soc. 2010, 132, 13848-13857; – reference: C. H. Lee, D. K. Dogutan, D. G. Nocera, J. Am. Chem. Soc. 2011, 133, 8775-8777; – reference: D. K. Dogutan, R. McGuire, Jr., D. G. Nocera, J. Am. Chem. Soc. 2011, 133, 9178-9180. – reference: I. Pochorovski, M.-O. Ebert, J.-P. Gisselbrecht, C. Boudon, W. B. Schweizer, F. Diederich, J. Am. Chem. Soc. 2012, 134, 14702-14705. – reference: K. Hiratani, M. Albrecht, Chem. Soc. Rev. 2008, 37, 2413-2421; – reference: V. M. Miskowski, V. H. Houlding, Inorg. Chem. 1991, 30, 4446-4452; – reference: E. Ohta, H. Sato, S. Ando, A. Kosaka, T. Fukushima, D. Hashizume, M. Yamasaki, K. Hasegawa, A. Muraoka, H. Ushiyama, K. Yamashita, T. Aida, Nat. Chem. 2011, 3, 68-73. – reference: C.-M. Che, S.-C. Chan, H.-F. Xiang, M. C. W. Chan, Y. Liu, Y. Wang, Chem. Commun. 2004, 1484-1485; – reference: S. Sun, W.-L. Tong, M. C. W. Chan, Macromol. Rapid Commun. 2010, 31, 1965-1969. – reference: A. J. Gallant, M. J. MacLachlan, Angew. Chem. 2003, 115, 5465-5468; – reference: T. Nakano, T. Yade, J. Am. Chem. Soc. 2003, 125, 15474-15484; – reference: S. M. H. Kabir, M. Hasegawa, Y. Kuwatani, M. Yoshida, H. Matsuyama, M. Iyoda, J. Chem. Soc. Perkin Trans. 1 2001, 159-165. – reference: J. H. Chong, S. Jooya Ardakani, K. J. Smith, M. J. MacLachlan, Chem. Eur. J. 2009, 15, 11824-11828; – reference: J. A. A. W. Elemans, S. J. Wezenberg, M. J. J. Coenen, E. C. Escudero-Adán, J. Benet-Buchholz, D. den Boer, S. Speller, A. W. Kleij, S. De Feyter, Chem. Commun. 2010, 46, 2548-2550. – reference: F. H. Zelder, J. Rebek Jr., Chem. Commun. 2006, 753-754; – reference: J. Rosenthal, T. D. Luckett, J. M. Hodgkiss, D. G. Nocera, J. Am. Chem. Soc. 2006, 128, 6546-6547; – reference: S.-Y. Liu, D. G. Nocera, J. Am. Chem. Soc. 2005, 127, 5278-5279; – reference: J. V. Mello, N. S. Finney, J. Am. Chem. Soc. 2005, 127, 10124-10125; – reference: F. Cozzi, F. Ponzini, R. Annunziata, M. Cinquini, J. S. Siegel, Angew. Chem. 1995, 107, 1092-1094; – reference: J. K.-H. Hui, Z. Yu, T. Mirfakhrai, M. J. MacLachlan, Chem. Eur. J. 2009, 15, 13456-13465; – reference: E. R. Libra, M. J. Scott, Chem. Commun. 2006, 1485-1487; – reference: J.-M. Lehn, Angew. Chem. 1988, 100, 91-116; – reference: M. D. Pluth, R. G. Bergman, K. N. Raymond, Acc. Chem. Res. 2009, 42, 1650-1659. – reference: H. J. Yoon, C. A. Mirkin, J. Am. Chem. Soc. 2008, 130, 11590-11591; – reference: S.-W. Lai, M. C. W. Chan, T.-C. Cheung, S.-M. Peng, C.-M. Che, Inorg. Chem. 1999, 38, 4046-4055; – reference: E. Benaksas Schwartz, C. B. Knobler, D. J. Cram, J. Am. Chem. Soc. 1992, 114, 10775-10784; – reference: C.-T. Chen, Y.-H. Lin, T.-S. Kuo, J. Am. Chem. Soc. 2008, 130, 12842-12843. – reference: L. Carbonaro, M. Isola, P. La Pegna, L. Senatore, F. Marchetti, Inorg. Chem. 1999, 38, 5519-5525. – reference: A. C. W. Leung, M. J. MacLachlan, J. Mater. Chem. 2007, 17, 1923-1932. – reference: T. J. Dunn, C. F. Ramogida, C. Simmonds, A. Paterson, E. W. Y. Wong, L. Chiang, Y. Shimazaki, T. Storr, Inorg. Chem. 2011, 50, 6746-6755; – reference: M. Shibasaki, M. Kanai, S. Matsunaga, N. Kumagai, Acc. Chem. Res. 2009, 42, 1117-1127; – reference: M. V. Escárcega-Bobadilla, G. Salassa, M. Martínez Belmonte, E. C. Escudero-Adán, A. W. Kleij, Chem. Eur. J. 2012, 18, 6805-6810. – reference: Angew. Chem. Int. Ed. 2005, 44, 4178-4182; – reference: M. Taherimehr, A. Decortes, S. M. Al-Amsyar, W. Lueangchaichaweng, C. J. Whiteoak, E. C. Escudero-Adán, A. W. Kleij, P. P. Pescarmona, Catal. Sci. Technol. 2012, 2, 2231-2237. – reference: F.-G. Klärner, B. Kahlert, Acc. Chem. Res. 2003, 36, 919-932; – reference: S. I. Vagin, R. Reichardt, S. Klaus, B. Rieger, J. Am. Chem. Soc. 2010, 132, 14367-14369; – reference: M. Barboiu, L. Prodi, M. Montalti, N. Zaccheroni, N. Kyritsakas, J.-M. Lehn, Chem. Eur. J. 2004, 10, 2953-2959; – reference: P. C. B. Widger, S. M. Ahmed, G. W. Coates, Macromolecules 2011, 44, 5666-5670. – reference: P. D. Frischmann, J. Jiang, J. K.-H. Hui, J. J. Grzybowski, M. J. MacLachlan, Org. Lett. 2008, 10, 1255-1258; – reference: K. Nakano, S. Hashimoto, K. Nozaki, Chem. Sci. 2010, 1, 369-373; – reference: C.-M. Che, C.-C. Kwok, S.-W. Lai, A. F. Rausch, W. J. Finkenzeller, N. Zhu, H. Yersin, Chem. Eur. J. 2010, 16, 233-247. – reference: G. Li, W. Yu, J. Ni, T. Liu, Y. Liu, E. Sheng, Y. Cui, Angew. Chem. 2008, 120, 1265-1269; – reference: V. J. Chebny, R. Rathore, J. Am. Chem. Soc. 2007, 129, 8458-8465; – reference: P. D. Frischmann, S. Guieu, R. Tabeshi, M. J. MacLachlan, J. Am. Chem. Soc. 2010, 132, 7668-7675. – reference: J. Y. Yang, D. G. Nocera, J. Am. Chem. Soc. 2007, 129, 8192-8198. – reference: C. J. Whiteoak, G. Salassa, A. W. Kleij, Chem. Soc. Rev. 2012, 41, 622-631. – reference: W. Lu, M. C. W. Chan, K.-K. Cheung, C.-M. Che, Organometallics 2001, 20, 2477-2486. – reference: N. Komiya, T. Muraoka, M. Iida, M. Miyanaga, K. Takahashi, T. Naota, J. Am. Chem. Soc. 2011, 133, 16054-16061. – reference: K.-H. Wong, M. C. W. Chan, C.-M. Che, Chem. Eur. J. 1999, 5, 2845-2849; – reference: S. D. Cummings, R. Eisenberg, J. Am. Chem. Soc. 1996, 118, 1949-1960. – reference: M. Cametti, M. Nissinen, A. Dalla Cort, L. Mandolini, K. Rissanen, J. Am. Chem. Soc. 2005, 127, 3831-3837; – reference: C. T. L. Ma, M. J. MacLachlan, Angew. Chem. 2005, 117, 4250-4254; – reference: A. W. Kleij, Chem. Eur. J. 2008, 14, 10520-10529; – reference: A. Rajca, A. Safronov, S. Rajca, C. R. Ross II, J. J. Stezowski, J. Am. Chem. Soc. 1996, 118, 7272-7279. – reference: K. E. Splan, A. M. Massari, G. A. Morris, S.-S. Sun, E. Reina, S. T. Nguyen, J. T. Hupp, Eur. J. Inorg. Chem. 2003, 2348-2351; – reference: A. C. W. Leung, J. K.-H. Hui, J. H. Chong, M. J. MacLachlan, Dalton Trans. 2009, 5199-5210; – reference: W.-L. Tong, M. C. W. Chan, S.-M. Yiu, Organometallics 2010, 29, 6377-6383. – reference: R. G. Konsler, J. Karl, E. N. Jacobsen, J. Am. Chem. Soc. 1998, 120, 10780-10781; – reference: Z. Guo, M. C. W. Chan, Chem. Eur. J. 2009, 15, 12585-12588. – reference: Angew. Chem. Int. Ed. Engl. 1995, 34, 1019-1020; – reference: W.-L. Tong, M. C. W. Chan, N. Zhu, S.-K. Leung, Dalton Trans. 2009, 4741-4746; – reference: T. J. Dunn, L. Chiang, C. F. Ramogida, M. I. Webb, D. Savard, M. Sakaguchi, T. Ogura, Y. Shimazaki, T. Storr, Dalton Trans. 2012, 41, 7905-7914. – reference: J. K.-H. Hui, P. D. Frischmann, C.-H. Tso, C. A. Michal, M. J. MacLachlan, Chem. Eur. J. 2010, 16, 2453-2460; – reference: D. P. Iwaniuk, C. Wolf, J. Am. Chem. Soc. 2011, 133, 2414-2417. – reference: N. C. Gianneschi, S.-H. Cho, S. T. Nguyen, C. A. Mirkin, Angew. Chem. 2004, 116, 5619-5623; – reference: Y.-Y. Lin, S.-C. Chan, M. C. W. Chan, Y.-J. Hou, N. Zhu, C.-M. Che, Y. Liu, Y. Wang, Chem. Eur. J. 2003, 9, 1263-1272; – reference: J. K.-H. Hui, M. J. MacLachlan, Chem. Commun. 2006, 2480-2482; – reference: Angew. Chem. Int. Ed. 2010, 49, 6430-6433; – reference: K. Rurack, U. Resch-Genger, Chem. Soc. Rev. 2002, 31, 116-127. – reference: W. Lu, M. C. W. Chan, N. Zhu, C.-M. Che, C. Li, Z. Hui, J. Am. Chem. Soc. 2004, 126, 7639-7651. – reference: M.-J. Li, C.-C. Ko, G.-P. Duan, N. Zhu, V. W.-W. Yam, Organometallics 2007, 26, 6091-6098; – reference: S. Dutta, D.-K. Bučar, L. R. MacGillivray, Org. Lett. 2011, 13, 2260-2262; – reference: Angew. Chem. Int. Ed. 2008, 47, 1245-1249; – reference: Y. Shen, B. P. Sullivan, Inorg. Chem. 1995, 34, 6235-6236; – reference: C. W. Chen, H. W. Whitlock, Jr., J. Am. Chem. Soc. 1978, 100, 4921-4922. – reference: H. Yoo, J. Yang, A. Yousef, M. R. Wasielewski, D. Kim, J. Am. Chem. Soc. 2010, 132, 3939-3944; – reference: T.-Q. Nguyen, R. Martel, P. Avouris, M. L. Bushey, L. Brus, C. Nuckolls, J. Am. Chem. Soc. 2004, 126, 5234-5242; – reference: J. Dömer, J. C. Slootweg, F. Hupka, K. Lammertsma, F. E. Hahn, Angew. Chem. 2010, 122, 6575-6578; – reference: J. R. Berenguer, A. Díez, J. Fernández, J. Forniés, A. García, B. Gil, E. Lalinde, M. T. Moreno, Inorg. Chem. 2008, 47, 7703-7716. – reference: B. A. Rodriguez, M. Delferro, T. J. Marks, J. Am. Chem. Soc. 2009, 131, 5902-5919; – reference: S. Guieu, A. K. Crane, M. J. MacLachlan, Chem. Commun. 2011, 47, 1169-1171. – reference: Angew. Chem. Int. Ed. 2004, 43, 5503-5507; – reference: W. Wu, J. Sun, S. Ji, W. Wu, J. Zhao, H. Guo, Dalton Trans. 2011, 40, 11550-11561. – reference: M. M. Elmahdy, X. Dou, M. Mondeshki, G. Floudas, H.-J. Butt, H. W. Spiess, K. Müllen, J. Am. Chem. Soc. 2008, 130, 5311-5319; – reference: Z. Guo, W.-L. Tong, M. C. W. Chan, Chem. Commun. 2009, 6189-6191. – reference: Angew. Chem. Int. Ed. Engl. 1994, 33, 1537-1554; – reference: Angew. Chem. Int. Ed. Engl. 1988, 27, 89-112; – reference: P. D. Frischmann, G. A. Facey, P. Y. Ghi, A. J. Gallant, D. L. Bryce, F. Lelj, M. J. MacLachlan, J. Am. Chem. Soc. 2010, 132, 3893-3908; – reference: P. Wu, D.-L. Ma, C.-H. Leung, S.-C. Yan, N. Zhu, R. Abagyan, C.-M. Che, Chem. Eur. J. 2009, 15, 13008-13021. – reference: T. J. Wadas, Q.-M. Wang, Y.-J. Kim, C. Flaschenreim, T. N. Blanton, R. Eisenberg, J. Am. Chem. Soc. 2004, 126, 16841-16849; – reference: Angew. Chem. Int. Ed. 2011, 50, 713-716. – reference: H. Houjou, M. Ito, K. Araki, Inorg. Chem. 2009, 48, 10703-10707. – reference: J. S. Nowick, P. Ballester, F. Ebmeyer, J. Rebek, Jr., J. Am. Chem. Soc. 1990, 112, 8902-8906; – reference: A. J. Goshe, I. M. Steele, B. Bosnich, J. Am. Chem. Soc. 2003, 125, 444-451; – reference: M. Martínez Belmonte, S. J. Wezenberg, R. M. Haak, D. Anselmo, E. C. Escudero-Adán, J. Benet-Buchholz, A. W. Kleij, Dalton Trans. 2010, 39, 4541-4550; – reference: S. Ulrich, J.-M. Lehn, Chem. Eur. J. 2009, 15, 5640-5645; – reference: S. Akine, T. Taniguchi, T. Nabeshima, J. Am. Chem. Soc. 2006, 128, 15765-15774; – reference: T. Mizuno, W.-H. Wei, L. R. Eller, J. L. Sessler, J. Am. Chem. Soc. 2002, 124, 1134-1135; – reference: S. A. McFarland, N. S. Finney, J. Am. Chem. Soc. 2002, 124, 1178-1179; – reference: A. L. Balch, V. J. Catalano, M. A. Chatfield, J. K. Nagle, M. M. Olmstead, P. E. Reedy, Jr., J. Am. Chem. Soc. 1991, 113, 1252-1258. – reference: Y. Hong, J. W. Y. Lam, B. Z. Tang, Chem. Commun. 2009, 4332-4353. – reference: S. J. Wezenberg, G. Salassa, E. C. Escudero-Adán, J. Benet-Buchholz, A. W. Kleij, Angew. Chem. 2011, 123, 739-742; – reference: M.-L. Ho, Y.-M. Cheng, L.-C. Wu, P.-T. Chou, G.-H. Lee, F.-C. Hsu, Y. Chi, Polyhedron 2007, 26, 4886-4892. – reference: Angew. Chem. Int. Ed. 2003, 42, 5307-5310; – volume: 126 start-page: 16841 year: 2004 end-page: 16849 publication-title: J. Am. Chem. Soc. – volume: 2 start-page: 2231 year: 2012 end-page: 2237 publication-title: Catal. Sci. Technol. – volume: 126 start-page: 5234 year: 2004 end-page: 5242 publication-title: J. Am. Chem. Soc. – volume: 106 33 start-page: 1620 1537 year: 1994 1994 end-page: 1639 1554 publication-title: Angew. Chem. Angew. Chem. Int. Ed. Engl. – volume: 40 start-page: 11550 year: 2011 end-page: 11561 publication-title: Dalton Trans. – start-page: 4332 year: 2009 end-page: 4353 publication-title: Chem. Commun. – volume: 14 start-page: 10520 year: 2008 end-page: 10529 publication-title: Chem. Eur. J. – volume: 41 start-page: 622 year: 2012 end-page: 631 publication-title: Chem. Soc. Rev. – volume: 133 start-page: 8775 year: 2011 end-page: 8777 publication-title: J. Am. Chem. Soc. – volume: 3 start-page: 68 year: 2011 end-page: 73 publication-title: Nat. Chem. – volume: 34 start-page: 6235 year: 1995 end-page: 6236 publication-title: Inorg. Chem. – volume: 26 start-page: 4886 year: 2007 end-page: 4892 publication-title: Polyhedron – start-page: 4242 year: 2006 end-page: 4244 publication-title: Chem. Commun. – volume: 132 start-page: 7668 year: 2010 end-page: 7675 publication-title: J. Am. Chem. Soc. – volume: 117 44 start-page: 4250 4178 year: 2005 2005 end-page: 4254 4182 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 123 start-page: 1260 year: 2001 end-page: 1261 publication-title: J. Am. Chem. Soc. – volume: 42 start-page: 1117 year: 2009 end-page: 1127 publication-title: Acc. Chem. Res. – volume: 41 start-page: 7905 year: 2012 end-page: 7914 publication-title: Dalton Trans. – volume: 37 start-page: 2413 year: 2008 end-page: 2421 publication-title: Chem. Soc. Rev. – volume: 47 start-page: 1169 year: 2011 end-page: 1171 publication-title: Chem. Commun. – volume: 9 start-page: 1263 year: 2003 end-page: 1272 publication-title: Chem. Eur. J. – volume: 16 start-page: 233 year: 2010 end-page: 247 publication-title: Chem. Eur. J. – start-page: 1484 year: 2004 end-page: 1485 publication-title: Chem. Commun. – volume: 112 start-page: 8902 year: 1990 end-page: 8906 publication-title: J. Am. Chem. Soc. – volume: 125 start-page: 444 year: 2003 end-page: 451 publication-title: J. Am. Chem. Soc. – volume: 132 start-page: 13848 year: 2010 end-page: 13857 publication-title: J. Am. Chem. Soc. – volume: 107 34 start-page: 1092 1019 year: 1995 1995 end-page: 1094 1020 publication-title: Angew. Chem. Angew. Chem. Int. Ed. Engl. – start-page: 753 year: 2006 end-page: 754 publication-title: Chem. Commun. – volume: 29 start-page: 6377 year: 2010 end-page: 6383 publication-title: Organometallics – volume: 134 start-page: 14702 year: 2012 end-page: 14705 publication-title: J. Am. Chem. Soc. – volume: 127 start-page: 5278 year: 2005 end-page: 5279 publication-title: J. Am. Chem. Soc. – volume: 100 27 start-page: 91 89 year: 1988 1988 end-page: 116 112 publication-title: Angew. Chem. Angew. Chem. Int. Ed. Engl. – volume: 132 start-page: 14367 year: 2010 end-page: 14369 publication-title: J. Am. Chem. Soc. – volume: 100 start-page: 4921 year: 1978 end-page: 4922 publication-title: J. Am. Chem. Soc. – volume: 48 start-page: 10703 year: 2009 end-page: 10707 publication-title: Inorg. Chem. – volume: 5 start-page: 2845 year: 1999 end-page: 2849 publication-title: Chem. Eur. J. – volume: 46 start-page: 2548 year: 2010 end-page: 2550 publication-title: Chem. Commun. – volume: 31 start-page: 1965 year: 2010 end-page: 1969 publication-title: Macromol. Rapid Commun. – start-page: 2348 year: 2003 end-page: 2351 publication-title: Eur. J. Inorg. Chem. – volume: 15 start-page: 12585 year: 2009 end-page: 12588 publication-title: Chem. Eur. J. – volume: 50 start-page: 6746 year: 2011 end-page: 6755 publication-title: Inorg. Chem. – volume: 15 start-page: 11824 year: 2009 end-page: 11828 publication-title: Chem. Eur. J. – volume: 127 start-page: 3831 year: 2005 end-page: 3837 publication-title: J. Am. Chem. Soc. – volume: 126 start-page: 7639 year: 2004 end-page: 7651 publication-title: J. Am. Chem. Soc. – volume: 38 start-page: 4046 year: 1999 end-page: 4055 publication-title: Inorg. Chem. – volume: 118 start-page: 1949 year: 1996 end-page: 1960 publication-title: J. Am. Chem. Soc. – volume: 38 start-page: 5519 year: 1999 end-page: 5525 publication-title: Inorg. Chem. – volume: 115 42 start-page: 5465 5307 year: 2003 2003 end-page: 5468 5310 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – start-page: 2480 year: 2006 end-page: 2482 publication-title: Chem. Commun. – volume: 15 start-page: 13456 year: 2009 end-page: 13465 publication-title: Chem. Eur. J. – volume: 47 start-page: 7703 year: 2008 end-page: 7716 publication-title: Inorg. Chem. – volume: 124 start-page: 1134 year: 2002 end-page: 1135 publication-title: J. Am. Chem. Soc. – volume: 116 43 start-page: 5619 5503 year: 2004 2004 end-page: 5623 5507 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 18 start-page: 6805 year: 2012 end-page: 6810 publication-title: Chem. Eur. J. – start-page: 6189 year: 2009 end-page: 6191 publication-title: Chem. Commun. – volume: 130 start-page: 12842 year: 2008 end-page: 12843 publication-title: J. Am. Chem. Soc. – volume: 133 start-page: 2414 year: 2011 end-page: 2417 publication-title: J. Am. Chem. Soc. – volume: 132 start-page: 3939 year: 2010 end-page: 3944 publication-title: J. Am. Chem. Soc. – volume: 34 start-page: 4591 year: 1995 end-page: 4599 publication-title: Inorg. Chem. – volume: 26 start-page: 6091 year: 2007 end-page: 6098 publication-title: Organometallics – volume: 129 start-page: 8192 year: 2007 end-page: 8198 publication-title: J. Am. Chem. Soc. – volume: 10 start-page: 2953 year: 2004 end-page: 2959 publication-title: Chem. Eur. J. – volume: 120 47 start-page: 1265 1245 year: 2008 2008 end-page: 1269 1249 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 133 start-page: 9178 year: 2011 end-page: 9180 publication-title: J. Am. Chem. Soc. – volume: 128 start-page: 15765 year: 2006 end-page: 15774 publication-title: J. Am. Chem. Soc. – volume: 130 start-page: 11590 year: 2008 end-page: 11591 publication-title: J. Am. Chem. Soc. – volume: 1 start-page: 369 year: 2010 end-page: 373 publication-title: Chem. Sci. – volume: 113 start-page: 1252 year: 1991 end-page: 1258 publication-title: J. Am. Chem. Soc. – volume: 114 start-page: 10775 year: 1992 end-page: 10784 publication-title: J. Am. Chem. Soc. – volume: 39 start-page: 4541 year: 2010 end-page: 4550 publication-title: Dalton Trans. – start-page: 1485 year: 2006 end-page: 1487 publication-title: Chem. Commun. – start-page: 5199 year: 2009 end-page: 5210 publication-title: Dalton Trans. – volume: 133 start-page: 16054 year: 2011 end-page: 16061 publication-title: J. Am. Chem. Soc. – volume: 17 start-page: 1923 year: 2007 end-page: 1932 publication-title: J. Mater. Chem. – volume: 131 start-page: 5902 year: 2009 end-page: 5919 publication-title: J. Am. Chem. Soc. – volume: 13 start-page: 2260 year: 2011 end-page: 2262 publication-title: Org. Lett. – start-page: 4741 year: 2009 end-page: 4746 publication-title: Dalton Trans. – volume: 127 start-page: 10124 year: 2005 end-page: 10125 publication-title: J. Am. Chem. Soc. – volume: 128 start-page: 6546 year: 2006 end-page: 6547 publication-title: J. Am. Chem. Soc. – volume: 122 49 start-page: 6575 6430 year: 2010 2010 end-page: 6578 6433 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 129 start-page: 8458 year: 2007 end-page: 8465 publication-title: J. Am. Chem. Soc. – volume: 120 start-page: 10780 year: 1998 end-page: 10781 publication-title: J. Am. Chem. Soc. – start-page: 159 year: 2001 end-page: 165 publication-title: J. Chem. Soc. Perkin Trans. 1 – volume: 44 start-page: 5666 year: 2011 end-page: 5670 publication-title: Macromolecules – volume: 42 start-page: 1650 year: 2009 end-page: 1659 publication-title: Acc. Chem. Res. – volume: 31 start-page: 116 year: 2002 end-page: 127 publication-title: Chem. Soc. Rev. – volume: 130 start-page: 5311 year: 2008 end-page: 5319 publication-title: J. Am. Chem. Soc. – volume: 36 start-page: 919 year: 2003 end-page: 932 publication-title: Acc. Chem. Res. – volume: 20 start-page: 2477 year: 2001 end-page: 2486 publication-title: Organometallics – volume: 132 start-page: 3893 year: 2010 end-page: 3908 publication-title: J. Am. Chem. Soc. – volume: 10 start-page: 1255 year: 2008 end-page: 1258 publication-title: Org. Lett. – volume: 16 start-page: 2453 year: 2010 end-page: 2460 publication-title: Chem. Eur. J. – volume: 118 start-page: 7272 year: 1996 end-page: 7279 publication-title: J. Am. Chem. Soc. – volume: 123 50 start-page: 739 713 year: 2011 2011 end-page: 742 716 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 15 start-page: 13008 year: 2009 end-page: 13021 publication-title: Chem. Eur. J. – volume: 30 start-page: 4446 year: 1991 end-page: 4452 publication-title: Inorg. Chem. – volume: 125 start-page: 15474 year: 2003 end-page: 15484 publication-title: J. Am. Chem. Soc. – volume: 15 start-page: 5640 year: 2009 end-page: 5645 publication-title: Chem. Eur. J. – volume: 124 start-page: 1178 year: 2002 end-page: 1179 publication-title: J. Am. Chem. Soc. – ident: e_1_2_6_19_2 – ident: e_1_2_6_22_2 doi: 10.1039/b517944k – ident: e_1_2_6_108_2 doi: 10.1021/ja961065y – ident: e_1_2_6_112_2 doi: 10.1021/ic00023a032 – ident: e_1_2_6_82_2 doi: 10.1002/chem.200306045 – ident: e_1_2_6_122_2 – ident: e_1_2_6_52_2 doi: 10.1021/ja804076q – ident: e_1_2_6_16_2 doi: 10.1002/ange.201002776 – ident: e_1_2_6_39_2 doi: 10.1039/b515558d – ident: e_1_2_6_104_2 doi: 10.1039/b402318h – ident: e_1_2_6_37_2 doi: 10.1021/ja070358w – ident: e_1_2_6_116_2 doi: 10.1021/ja951345y – ident: e_1_2_6_53_2 doi: 10.1021/ja900257k – ident: e_1_2_6_35_2 – ident: e_1_2_6_57_2 doi: 10.1039/b100604p – ident: e_1_2_6_21_2 doi: 10.1021/ja0646702 – ident: e_1_2_6_25_2 doi: 10.1039/b925560e – ident: e_1_2_6_79_2 – ident: e_1_2_6_59_2 doi: 10.1002/ange.19941061505 – ident: e_1_2_6_70_2 doi: 10.1021/ja058731s – ident: e_1_2_6_6_2 doi: 10.1002/chem.200801149 – ident: e_1_2_6_20_2 doi: 10.1021/ja042807n – ident: e_1_2_6_44_2 doi: 10.1021/ic901937p – ident: e_1_2_6_55_2 doi: 10.1039/c0sc00220h – ident: e_1_2_6_41_2 doi: 10.1039/c2cy20171b – ident: e_1_2_6_88_2 doi: 10.1021/ja028910z – ident: e_1_2_6_98_2 – ident: e_1_2_6_110_2 – ident: e_1_2_6_18_2 doi: 10.1002/chem.201200335 – ident: e_1_2_6_30_2 doi: 10.1021/ja910886g – ident: e_1_2_6_12_2 doi: 10.1039/C0CC04493H – ident: e_1_2_6_17_2 doi: 10.1021/ja910419h – ident: e_1_2_6_66_2 doi: 10.1021/ja7113618 – ident: e_1_2_6_40_2 doi: 10.1021/ar9000108 – ident: e_1_2_6_28_2 doi: 10.1002/chem.200902031 – ident: e_1_2_6_83_2 doi: 10.1021/ja043682p – ident: e_1_2_6_61_2 doi: 10.1021/ja00053a014 – ident: e_1_2_6_90_2 doi: 10.1002/chem.200900238 – ident: e_1_2_6_68_2 doi: 10.1038/nchem.900 – ident: e_1_2_6_115_2 doi: 10.1021/ja039727o – ident: e_1_2_6_65_2 doi: 10.1021/ja031600b – ident: e_1_2_6_77_2 doi: 10.1021/ol200532t – ident: e_1_2_6_14_2 doi: 10.1002/ange.200500058 – ident: e_1_2_6_113_2 doi: 10.1021/ic00122a015 – ident: e_1_2_6_60_2 doi: 10.1021/ja00180a038 – ident: e_1_2_6_56_2 doi: 10.1021/ma201078m – ident: e_1_2_6_78_2 doi: 10.1021/ja111583e – ident: e_1_2_6_121_2 doi: 10.1016/j.poly.2007.06.029 – ident: e_1_2_6_43_2 doi: 10.1002/ejic.200200665 – ident: e_1_2_6_47_2 doi: 10.1021/ic200785g – ident: e_1_2_6_31_2 doi: 10.1039/b618833h – ident: e_1_2_6_2_3 doi: 10.1002/anie.198800891 – ident: e_1_2_6_32_2 – ident: e_1_2_6_33_3 doi: 10.1002/anie.200704347 – ident: e_1_2_6_101_2 doi: 10.1002/chem.200901943 – ident: e_1_2_6_38_2 – ident: e_1_2_6_51_2 doi: 10.1021/ja982683c – ident: e_1_2_6_73_2 – ident: e_1_2_6_74_3 doi: 10.1002/anie.199510191 – ident: e_1_2_6_105_2 doi: 10.1002/chem.200902183 – ident: e_1_2_6_59_3 doi: 10.1002/anie.199415371 – ident: e_1_2_6_54_2 doi: 10.1021/ja106484t – ident: e_1_2_6_45_2 – ident: e_1_2_6_33_2 doi: 10.1002/ange.200704347 – ident: e_1_2_6_118_2 – ident: e_1_2_6_42_2 – ident: e_1_2_6_2_2 doi: 10.1002/ange.19881000110 – ident: e_1_2_6_81_2 doi: 10.1021/ja017309i – ident: e_1_2_6_87_2 doi: 10.1021/ar0200448 – ident: e_1_2_6_1_2 – ident: e_1_2_6_97_2 doi: 10.1002/marc.201000266 – ident: e_1_2_6_86_2 – ident: e_1_2_6_128_2 – ident: e_1_2_6_58_2 – ident: e_1_2_6_74_2 doi: 10.1002/ange.19951070914 – ident: e_1_2_6_27_2 – ident: e_1_2_6_13_2 – ident: e_1_2_6_8_2 – ident: e_1_2_6_64_2 doi: 10.1021/ja037836x – ident: e_1_2_6_85_2 doi: 10.1021/ja00483a063 – ident: e_1_2_6_29_2 doi: 10.1002/chem.200902712 – ident: e_1_2_6_94_2 doi: 10.1039/b900030e – ident: e_1_2_6_89_3 doi: 10.1002/anie.200460932 – ident: e_1_2_6_100_2 doi: 10.1002/(SICI)1521-3765(19991001)5:10<2845::AID-CHEM2845>3.0.CO;2-G – ident: e_1_2_6_119_2 doi: 10.1021/ic00129a003 – ident: e_1_2_6_80_2 doi: 10.1021/ja005701a – ident: e_1_2_6_62_2 doi: 10.1039/b904665h – ident: e_1_2_6_89_2 doi: 10.1002/ange.200460932 – ident: e_1_2_6_114_2 doi: 10.1021/ja047955s – ident: e_1_2_6_71_2 doi: 10.1021/ja202136y – ident: e_1_2_6_34_3 doi: 10.1002/anie.201004957 – ident: e_1_2_6_11_2 doi: 10.1021/ol8001317 – ident: e_1_2_6_106_2 doi: 10.1039/c1dt11001b – ident: e_1_2_6_7_2 doi: 10.1039/C1CS15170C – ident: e_1_2_6_26_2 doi: 10.1039/b922212j – ident: e_1_2_6_93_2 – ident: e_1_2_6_34_2 doi: 10.1002/ange.201004957 – ident: e_1_2_6_124_2 doi: 10.1021/ic990189j – ident: e_1_2_6_91_2 doi: 10.1021/ja910724x – ident: e_1_2_6_126_2 doi: 10.1021/ja00004a027 – ident: e_1_2_6_10_2 doi: 10.1039/b603985e – ident: e_1_2_6_14_3 doi: 10.1002/anie.200500058 – ident: e_1_2_6_36_2 doi: 10.1021/ja042849b – ident: e_1_2_6_102_2 – ident: e_1_2_6_117_2 doi: 10.1021/om0009839 – ident: e_1_2_6_109_2 doi: 10.1039/b006375o – ident: e_1_2_6_23_2 doi: 10.1021/ja8051552 – ident: e_1_2_6_4_2 doi: 10.1021/ar900118t – ident: e_1_2_6_67_2 doi: 10.1021/ja106050s – ident: e_1_2_6_127_2 – ident: e_1_2_6_99_2 doi: 10.1021/ic990238s – ident: e_1_2_6_5_2 – ident: e_1_2_6_125_2 doi: 10.1021/ic8006876 – ident: e_1_2_6_9_2 doi: 10.1002/ange.200352395 – ident: e_1_2_6_24_2 – ident: e_1_2_6_96_2 doi: 10.1002/chem.200902328 – ident: e_1_2_6_63_2 – ident: e_1_2_6_69_2 – ident: e_1_2_6_95_2 doi: 10.1021/om1007488 – ident: e_1_2_6_76_2 doi: 10.1021/ja0687522 – ident: e_1_2_6_103_2 doi: 10.1002/chem.200390143 – ident: e_1_2_6_107_2 doi: 10.1039/b909645k – ident: e_1_2_6_50_2 – ident: e_1_2_6_120_2 doi: 10.1021/om700481f – ident: e_1_2_6_9_3 doi: 10.1002/anie.200352395 – ident: e_1_2_6_3_2 doi: 10.1039/b719548f – ident: e_1_2_6_111_2 – ident: e_1_2_6_49_2 doi: 10.1021/ja2039369 – ident: e_1_2_6_75_2 doi: 10.1021/ja017298t – ident: e_1_2_6_92_2 doi: 10.1021/ja306473x – ident: e_1_2_6_84_2 doi: 10.1039/b609880k – ident: e_1_2_6_72_2 doi: 10.1021/ja202138m – ident: e_1_2_6_15_2 doi: 10.1002/chem.200902188 – ident: e_1_2_6_123_2 – ident: e_1_2_6_46_2 doi: 10.1039/b903963e – ident: e_1_2_6_48_2 doi: 10.1039/c2dt30444a – ident: e_1_2_6_16_3 doi: 10.1002/anie.201002776 |
| SSID | ssj0009633 |
| Score | 2.2605326 |
| Snippet | The development of molecular frameworks derived from binuclear platinum(II) aromatic Schiff base (salphen) complexes and their supramolecular chemistry have... |
| SourceID | proquest pubmed crossref wiley istex |
| SourceType | Aggregation Database Index Database Enrichment Source Publisher |
| StartPage | 8937 |
| SubjectTerms | Chemistry Comparative studies Crystallography Emissions luminescence pi interactions platinum Proteins sensors supramolecular chemistry |
| Title | Shape-Persistent (Pt-salphen)2 Phosphorescent Coordination Frameworks: Structural Insights and Selective Perturbations |
| URI | https://api.istex.fr/ark:/67375/WNG-PK3RZXCQ-N/fulltext.pdf https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fchem.201300421 https://www.ncbi.nlm.nih.gov/pubmed/23682037 https://www.proquest.com/docview/1370164072 https://www.proquest.com/docview/1371270580 |
| Volume | 19 |
| hasFullText | 1 |
| inHoldings | 1 |
| isFullTextHit | |
| isPrint | |
| link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9QwEB6hcoAL70fagoyEeBzS5uHECTe0YikgVkuXihUXK45tLSpKVs1WQj3xE_iN_BJm7E3KIhAS3JJ4rPgxtr-xx98APOQGl7XYGhzfKgq5LlRY1hqt1kppa22WW0fi-naSHxzx1_Ns_tMtfs8PMWy40chw8zUN8Ep1--ekoVgnuklOxzHc3SQnhy1CRYfn_FGoXT6WPBchcbD2rI1Rsr-ZfWNVukgN_OV3kHMTwbolaHwVqr7w3vPkeO90pfbqs194Hf-ndtfgyhqfsudeoa7DBdPcgEujPizcTTibLaql-f71G_nOUxWaFXsyXeGHju7tmuZpwqaLtlsu2hNPFcVGLVq4n_y2Ixv33mDdMzZz5LVE_MFeNR1tE3SsajSbueA8OA8z_AmmK7-teAuOxi_ejw7CdQCHsOZCxGGcGTRSEYClFGM9LoyyeV6qksc1AidUDm20ziKj8ElwW1peG8QzKo2MUIXN0tuw1bSNuQusLGqT2aQkbh9udKziqLBFjbZBTCEddABh34GyXrObU5CNz9LzMieSWlQOLRrA40F-6Xk9_ij5yOnDIFadHJM3nMjkh8lLOX2THn6cj97JSQC7vcLI9UTQyTgVRGIWiSSAB0Mydhmdy1SNaU-dDJ3_Z0UUwB2vaMPPkjRHjJaKABKnLn8prCQijeFt-18y7cDlxIX8IJfkXdhCTTD3EHit1H03uH4AO3gmgw |
| linkProvider | Wiley-Blackwell |
| linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9QwEB6h9lAuvB8pBYyEeBzSxonz4oZWLFvarpZuKyouVpzYWtQqWTVbCfXET-A38kuYsTepFoGQ4JbEtuLH2J4Zj78P4LnQuK1xo3F-q8AXVab8vKzQai1UZYyJE2NBXA_GyehYfDiJu2hCugvj8CF6hxvNDLte0wQnh_TOFWooNoquktN5jKCr5OtE622tqsMrBCmUL8cmL1KfUFg73MYg3Fktv7IvrVMXf_2d0rmqw9pNaHgTVFd9F3tyun2xUNvl5S_Ijv_VvltwY6misrdOpm7DNV3fgY1Bxwx3Fy6ns2Kuf3z7TuHz1IZ6wV5NFvihpau7un4dssmsaeez5tyhRbFBg0buF-d5ZMMuIKx9w6YWv5awP9hu3ZKnoGVFXbGp5efBpZjhTzBdOc_iPTgevjsajPwlh4NfijTlPo812qmog0VEs84zrUyS5CoXvETdCeWj0lUVB1rhUypMbkSpUaVRUaBTlZk4ug9rdVPrh8DyrNSxCXOC9xG64ooHmclKNA84sTpUHvjdCMpyCXBOPBtn0kEzh5J6VPY96sHLPv_cQXv8MecLKxB9tuL8lALi0lh-Gr-Xk73o8PPJ4KMce7DVSYxcrgWt5FFKOGZBGnrwrE_GIaOjmaLWzYXNQyEAcRZ48MBJWv-zMEpQTYtSD0IrL3-prCQsjf5t818KPYWN0dHBvtzfHe89guuhZQChCOUtWEOp0I9RD1uoJ3am_QSPByqe |
| linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9QwEB6hVgIuUN6BAkZCPA5p83Be3NCWpaWwWrpUrLhYcWxrUVGyarZS1RM_gd_IL2HG3qQsAiHBLYnHih_f2GN7_A3AY65xWguNRv2Wgc9VLv2iUrhqLaUyxiSpsSSu70bp7iF_M02mP93id_wQ_YYbaYYdr0nB58psn5OGYp3oJjkdx3C6Sb7O0yAnXO8cnBNIIbxcMHme-UTC2tE2BtH2av6VaWmdWvj0dzbnqglr56DhVSi70jvXk6Otk4Xcqs5-IXb8n-ptwJWlgcpeOkRdgwu6vg6XBl1cuBtwNpmVc_396zdynqcq1Av2bLzADy1d3NX184iNZ007nzXHjiuKDRpc4n52-45s2LmDtS_YxLLXEvMH26tb2idoWVkrNrHReXAgZvgTTJduX_EmHA5ffRjs-ssIDn7Fsyz0w0TjKhUtsJiCrIe5liZNC1nwsELLCdGhtFJJoCU-ZdwUhlcaDRoZBzqTuUniW7BWN7W-A6zIK52YqCByH65VKMMgN3mFi4OQYjooD_yuA0W1pDenKBtfhCNmjgS1qOhb1IOnvfzcEXv8UfKJxUMvVh4fkTtcloiPo9divB8ffJoO3ouRB5sdYMRyJGhFGGfEYhZkkQeP-mTsMjqYKWvdnFgZcgBI8sCD2w5o_c-iOEUjLc48iCxc_lJYQUwa_dvdf8n0EC6Od4bi7d5o_x5cjmz4D3JP3oQ1BIW-j0bYQj6wevYDCg0pVg |
| openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Shape%E2%80%90Persistent+%28Pt%E2%80%90salphen%292+Phosphorescent+Coordination+Frameworks%3A+Structural+Insights+and+Selective+Perturbations&rft.jtitle=Chemistry+%3A+a+European+journal&rft.au=Guo%2C+Zhengqing&rft.au=Yiu%2C+Shek%E2%80%90Man&rft.au=Chan%2C+Michael+C.+W.&rft.date=2013-07-01&rft.pub=WILEY%E2%80%90VCH+Verlag&rft.issn=0947-6539&rft.eissn=1521-3765&rft.volume=19&rft.issue=27&rft.spage=8937&rft.epage=8947&rft_id=info:doi/10.1002%2Fchem.201300421&rft.externalDBID=10.1002%252Fchem.201300421&rft.externalDocID=CHEM201300421 |
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0947-6539&client=summon |
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0947-6539&client=summon |
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0947-6539&client=summon |