Hydrolytic Conversion of a Metal-Organic Polyhedron into a Metal-Organic Framework
Twist and release: The metal–organic polyhedron 1 synthesized from 5‐(prop‐2‐ynyloxy)isophthalic acid and Cu(NO3)2⋅ 3 H2O has a hydrophobic outer surface and a hydrophilic inner core. In an aqueous medium, the resulting polarity gradient led to the transformation of 1 into the 2D metal–organic frame...
Saved in:
| Published in | Angewandte Chemie International Edition Vol. 52; no. 51; pp. 13755 - 13759 |
|---|---|
| Main Authors | , , , |
| Format | Journal Article |
| Language | English |
| Published |
Weinheim
WILEY-VCH Verlag
16.12.2013
WILEY‐VCH Verlag Wiley Subscription Services, Inc |
| Edition | International ed. in English |
| Subjects | |
| Online Access | Get full text |
Cover
Loading…
| Abstract | Twist and release: The metal–organic polyhedron 1 synthesized from 5‐(prop‐2‐ynyloxy)isophthalic acid and Cu(NO3)2⋅ 3 H2O has a hydrophobic outer surface and a hydrophilic inner core. In an aqueous medium, the resulting polarity gradient led to the transformation of 1 into the 2D metal–organic framework 2. This unique phenomenon enabled the gradual release of entrapped drug molecules. |
|---|---|
| AbstractList | Twist and release: The metal-organic polyhedron 1 synthesized from 5-(prop-2-ynyloxy)isophthalic acid and Cu(NO3 )2 ⋅ 3 H2 O has a hydrophobic outer surface and a hydrophilic inner core. In an aqueous medium, the resulting polarity gradient led to the transformation of 1 into the 2D metal-organic framework 2. This unique phenomenon enabled the gradual release of entrapped drug molecules.Twist and release: The metal-organic polyhedron 1 synthesized from 5-(prop-2-ynyloxy)isophthalic acid and Cu(NO3 )2 ⋅ 3 H2 O has a hydrophobic outer surface and a hydrophilic inner core. In an aqueous medium, the resulting polarity gradient led to the transformation of 1 into the 2D metal-organic framework 2. This unique phenomenon enabled the gradual release of entrapped drug molecules. Twist and release: The metal-organic polyhedron 1 synthesized from 5-(prop-2-ynyloxy)isophthalic acid and Cu(NO3 )2 ⋅ 3 H2 O has a hydrophobic outer surface and a hydrophilic inner core. In an aqueous medium, the resulting polarity gradient led to the transformation of 1 into the 2D metal-organic framework 2. This unique phenomenon enabled the gradual release of entrapped drug molecules. Twist and release: The metal-organic polyhedron 1 synthesized from 5-(prop-2-ynyloxy)isophthalic acid and Cu(NO3 )2 3H2 O has a hydrophobic outer surface and a hydrophilic inner core. In an aqueous medium, the resulting polarity gradient led to the transformation of 1 into the 2D metal-organic framework 2. This unique phenomenon enabled the gradual release of entrapped drug molecules. Twist and release: The metal–organic polyhedron 1 synthesized from 5‐(prop‐2‐ynyloxy)isophthalic acid and Cu(NO3)2⋅ 3 H2O has a hydrophobic outer surface and a hydrophilic inner core. In an aqueous medium, the resulting polarity gradient led to the transformation of 1 into the 2D metal–organic framework 2. This unique phenomenon enabled the gradual release of entrapped drug molecules. Twist and release: The metal-organic polyhedron 1 synthesized from 5-(prop-2-ynyloxy)isophthalic acid and Cu(NO sub(3)) sub(2) 3H sub(2)O has a hydrophobic outer surface and a hydrophilic inner core. In an aqueous medium, the resulting polarity gradient led to the transformation of 1 into the 2D metal-organic framework 2. This unique phenomenon enabled the gradual release of entrapped drug molecules. |
| Author | Díaz, David Díaz Mallick, Arijit Banerjee, Rahul Garai, Bikash |
| Author_xml | – sequence: 1 givenname: Arijit surname: Mallick fullname: Mallick, Arijit organization: Physical/Materials Chemistry Division, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, Pune-411008 (India) – sequence: 2 givenname: Bikash surname: Garai fullname: Garai, Bikash organization: Physical/Materials Chemistry Division, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, Pune-411008 (India) – sequence: 3 givenname: David Díaz surname: Díaz fullname: Díaz, David Díaz organization: Institut für Organische Chemie, Universität Regensburg, Universitätsstrasse 31, 93040 Regensburg (Germany) – sequence: 4 givenname: Rahul surname: Banerjee fullname: Banerjee, Rahul email: r.banerjee@ncl.res.in organization: Physical/Materials Chemistry Division, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, Pune-411008 (India) |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24346950$$D View this record in MEDLINE/PubMed |
| BookMark | eNqFkctP3DAQh62Kqjzaa49VpF56yeJnnBzpCnaReKkEcbQcZ9wasjbY2dL97-vVAqpAFSdb8veNZ36zi7Z88IDQZ4InBGO6r72DCcWEYcnr6h3aIYKSkknJtvKdM1bKWpBttJvSTebrGlcf0DbljFeNwDvox3zVxzCsRmeKafC_ISYXfBFsoYtTGPVQnsef-RNTXGTqF2TYF86P4dX7UdQLeAjx9iN6b_WQ4NPjuYeujg7b6bw8OZ8dTw9OSsNrUpUceAe5Ud1YwNz2YGqwFJueWCMk4R3vQRhLGy1MZTte8b6muf2u6bSwgrI99G1T9y6G-yWkUS1cMjAM2kNYJkUkJoQyQeXbaE6jYg2hIqNfX6A3YRl9HmRN1VVOHfNMfXmklt0CenUX3ULHlXoKNgN8A5gYUopglXGjHnO2Y9RuUASr9f7Uen_qeX9Zm7zQnir_V2g2woMbYPUGrQ7Ojg__dcuN69IIf55dHW9VJZkU6vpspmZt287b79fqkv0FIDS73g |
| CODEN | ACIEAY |
| CitedBy_id | crossref_primary_10_1002_chem_201805808 crossref_primary_10_1021_acs_chemrev_9b00803 crossref_primary_10_1039_D3TA03300G crossref_primary_10_1021_acs_cgd_6b00853 crossref_primary_10_1021_acs_inorgchem_2c02046 crossref_primary_10_1002_adfm_201503154 crossref_primary_10_1016_j_ccr_2022_214612 crossref_primary_10_1039_C5CC03102H crossref_primary_10_1002_ange_201610914 crossref_primary_10_1039_C4CS00222A crossref_primary_10_1021_cg5018592 crossref_primary_10_1002_adma_202309570 crossref_primary_10_1016_j_ccr_2020_213679 crossref_primary_10_1021_jacs_5b10815 crossref_primary_10_1039_C8CE00537K crossref_primary_10_1002_ange_201309778 crossref_primary_10_1039_C9TA12497G crossref_primary_10_1039_D1TC00470K crossref_primary_10_1021_acs_inorgchem_1c03203 crossref_primary_10_1002_adma_201801399 crossref_primary_10_1002_chem_201905249 crossref_primary_10_1021_acs_inorgchem_7b00267 crossref_primary_10_1016_j_molstruc_2024_137911 crossref_primary_10_1021_acs_chemmater_8b01667 crossref_primary_10_1021_acs_chemmater_5b00084 crossref_primary_10_1002_chem_201501672 crossref_primary_10_1021_jacs_2c13798 crossref_primary_10_1021_jacs_6b01758 crossref_primary_10_1038_s41598_017_00733_4 crossref_primary_10_1021_cs501953d crossref_primary_10_1039_C8CC00130H crossref_primary_10_1039_C4CC09139F crossref_primary_10_1021_acs_chemmater_6b03030 crossref_primary_10_1039_D0CS00443J crossref_primary_10_3390_catal13020317 crossref_primary_10_1038_s41467_017_02736_1 crossref_primary_10_1039_C7TA01069A crossref_primary_10_1021_acs_inorgchem_9b00997 crossref_primary_10_1021_jacs_4c16021 crossref_primary_10_1038_s41467_018_05818_w crossref_primary_10_1039_C5CE00004A crossref_primary_10_1016_j_ica_2024_122297 crossref_primary_10_1039_C5CE01456E crossref_primary_10_1021_acsanm_2c04828 crossref_primary_10_1039_D3CE01251D crossref_primary_10_1002_asia_201900712 crossref_primary_10_1021_acs_chemmater_6b01898 crossref_primary_10_1002_anie_201600497 crossref_primary_10_1039_C8CE01003J crossref_primary_10_1002_chem_201801594 crossref_primary_10_1021_acs_chemmater_0c00851 crossref_primary_10_1002_chem_201700848 crossref_primary_10_1021_jacs_2c03402 crossref_primary_10_1002_cplu_202400169 crossref_primary_10_1016_j_inoche_2018_11_014 crossref_primary_10_1002_smll_202308393 crossref_primary_10_1021_acs_inorgchem_2c04078 crossref_primary_10_1002_anie_201610914 crossref_primary_10_1039_C4CS00033A crossref_primary_10_1039_C5CC01732G crossref_primary_10_1039_D0SC04941G crossref_primary_10_1021_acs_cgd_6b00805 crossref_primary_10_1002_ange_201600497 crossref_primary_10_1021_jacs_6b01414 crossref_primary_10_1002_asia_201900800 crossref_primary_10_1039_C5RA26357C crossref_primary_10_1039_C7CE00786H crossref_primary_10_1002_anie_201309778 crossref_primary_10_1021_acsami_8b02015 crossref_primary_10_1021_acs_jpcc_2c07644 crossref_primary_10_1039_C5GC02530C |
| Cites_doi | 10.1002/ange.200802240 10.1002/ange.201100193 10.1021/am301365h 10.1039/c1cc14523a 10.1002/anie.201105325 10.1039/C0CC02573A 10.1002/anie.200704924 10.1021/ja306150x 10.1039/c1cc11167a 10.1021/ja803783c 10.1002/anie.201100193 10.1038/nchem.803 10.1002/ange.201105325 10.1039/c1cc00030f 10.1002/ange.200704924 10.1039/b102714j 10.1039/C1SC00847A 10.1002/anie.200802240 10.1021/ja103109z 10.1021/cm400798p 10.1002/anie.201209694 10.1002/adma.201003012 10.1002/anie.201108731 10.1021/ja205450a 10.1002/ange.201202665 10.1002/ange.200904722 10.1126/science.1204369 10.1126/science.1175313 10.1002/ange.200705008 10.1002/ange.201209694 10.1002/anie.200904722 10.1021/ic7013623 10.1021/ja3063925 10.1021/ja1080794 10.1002/anie.200705008 10.1002/anie.201202665 10.1038/nchem.1031 10.1002/asia.201000842 10.1039/C0SC00523A 10.1021/ja0104352 10.1021/ja900676f 10.1039/b925335a 10.1038/nmat2608 10.1021/ja309949q 10.1126/science.1188605 10.1002/ange.201108731 10.1039/c003191g |
| 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 7TM K9. 7X8 7SR 8BQ 8FD JG9 |
| DOI | 10.1002/anie.201307486 |
| DatabaseName | Istex CrossRef PubMed Nucleic Acids Abstracts ProQuest Health & Medical Complete (Alumni) MEDLINE - Academic Engineered Materials Abstracts METADEX Technology Research Database Materials Research Database |
| DatabaseTitle | CrossRef PubMed ProQuest Health & Medical Complete (Alumni) Nucleic Acids Abstracts MEDLINE - Academic Materials Research Database Engineered Materials Abstracts Technology Research Database METADEX |
| DatabaseTitleList | MEDLINE - Academic PubMed ProQuest Health & Medical Complete (Alumni) Materials Research Database |
| 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 | 1521-3773 |
| Edition | International ed. in English |
| EndPage | 13759 |
| ExternalDocumentID | 3158264241 24346950 10_1002_anie_201307486 ANIE201307486 ark_67375_WNG_GTTTHTBW_S |
| Genre | shortCommunication Journal Article |
| GrantInformation_xml | – fundername: UGC, New Delhi, India – fundername: BRNS funderid: 2011/37C/44/BRNS – fundername: CSIR, New Delhi, India |
| GroupedDBID | --- -DZ -~X .3N .GA .Y3 05W 0R~ 10A 1L6 1OB 1OC 1ZS 23M 31~ 33P 3SF 3WU 4.4 4ZD 50Y 50Z 51W 51X 52M 52N 52O 52P 52S 52T 52U 52W 52X 53G 5GY 5RE 5VS 66C 6TJ 702 7PT 8-0 8-1 8-3 8-4 8-5 8UM 930 A03 AAESR AAEVG AAHHS AANLZ AAONW AASGY AAXRX AAZKR ABCQN ABCUV ABEML ABIJN ABLJU ABPPZ ABPVW ACAHQ ACBWZ ACCFJ ACCZN ACFBH ACGFS ACIWK ACNCT ACPOU ACPRK ACSCC ACXBN ACXQS ADBBV ADEOM ADIZJ ADKYN ADMGS ADOZA ADXAS ADZMN ADZOD AEEZP AEIGN AEIMD AEQDE AEUQT AEUYR AFBPY AFFNX AFFPM AFGKR AFPWT AFRAH AFZJQ AHBTC AHMBA AITYG AIURR AIWBW AJBDE AJXKR ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN AMBMR AMYDB ATUGU AUFTA AZBYB AZFZN AZVAB B-7 BAFTC BDRZF BFHJK BHBCM BMNLL BMXJE BNHUX BROTX BRXPI BSCLL BTSUX BY8 CS3 D-E D-F D0L DCZOG DPXWK DR1 DR2 DRFUL DRSTM 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 M53 MEWTI MK4 MRFUL MRSTM MSFUL MSSTM MXFUL MXSTM N04 N05 N9A NF~ NNB O66 O9- OIG P2P P2W P2X P4D PQQKQ Q.N Q11 QB0 QRW R.K RNS ROL RWI RX1 RYL SUPJJ TN5 UB1 UPT V2E VQA W8V W99 WBFHL WBKPD WH7 WIB WIH WIK WJL WOHZO WQJ WRC WXSBR WYISQ XG1 XPP XSW XV2 YZZ ZZTAW ~IA ~KM ~WT AAHQN AAMNL AANHP AAYCA ABDBF ABJNI ACRPL ACYXJ ADNMO AETEA AEYWJ AFWVQ AGQPQ AGYGG ALVPJ AAYXX CITATION NPM YIN 7TM K9. 7X8 7SR 8BQ 8FD JG9 |
| ID | FETCH-LOGICAL-c4816-4e4be377a9fe04fdec8ef20cd1fc5714b4de5cf29a5c6fb464d82806b9ba5f523 |
| IEDL.DBID | DR2 |
| ISSN | 1433-7851 1521-3773 |
| IngestDate | Fri Jul 11 11:56:10 EDT 2025 Fri Jul 11 00:16:47 EDT 2025 Fri Jul 25 10:40:37 EDT 2025 Wed Feb 19 01:52:18 EST 2025 Tue Jul 01 02:53:22 EDT 2025 Thu Apr 24 23:00:07 EDT 2025 Wed Aug 20 07:25:18 EDT 2025 Wed Oct 30 09:53:06 EDT 2024 |
| IsPeerReviewed | true |
| IsScholarly | true |
| Issue | 51 |
| Keywords | self-assembly cage compounds crystal engineering hydrophobic effect metal-organic frameworks |
| Language | English |
| License | http://onlinelibrary.wiley.com/termsAndConditions#vor Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
| LinkModel | DirectLink |
| MergedId | FETCHMERGED-LOGICAL-c4816-4e4be377a9fe04fdec8ef20cd1fc5714b4de5cf29a5c6fb464d82806b9ba5f523 |
| Notes | BRNS - No. 2011/37C/44/BRNS A.M. acknowledges the CSIR, New Delhi, India for a SRF, and B.G. acknowledges the UGC, New Delhi, India for a JRF. R.B. acknowledges the CSIR Five Year Plan (CSC0122 and CSC0102) for funding. Financial assistance from the BRNS (2011/37C/44/BRNS) is acknowledged. ArticleID:ANIE201307486 CSIR, New Delhi, India ark:/67375/WNG-GTTTHTBW-S istex:07EE59C69CA4AEB033914C6BF46ACF975AE6B0A2 UGC, New Delhi, India These authors contributed equally. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
| PMID | 24346950 |
| PQID | 1468610004 |
| PQPubID | 946352 |
| PageCount | 5 |
| ParticipantIDs | proquest_miscellaneous_1701123527 proquest_miscellaneous_1469639125 proquest_journals_1468610004 pubmed_primary_24346950 crossref_citationtrail_10_1002_anie_201307486 crossref_primary_10_1002_anie_201307486 wiley_primary_10_1002_anie_201307486_ANIE201307486 istex_primary_ark_67375_WNG_GTTTHTBW_S |
| ProviderPackageCode | CITATION AAYXX |
| PublicationCentury | 2000 |
| PublicationDate | December 16, 2013 |
| PublicationDateYYYYMMDD | 2013-12-16 |
| PublicationDate_xml | – month: 12 year: 2013 text: December 16, 2013 day: 16 |
| PublicationDecade | 2010 |
| PublicationPlace | Weinheim |
| PublicationPlace_xml | – name: Weinheim – name: Germany |
| PublicationTitle | Angewandte Chemie International Edition |
| PublicationTitleAlternate | Angew. Chem. Int. Ed |
| 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 | P. Mal, B. Breiner, K. Rissanen, J. R. Nitschke, Science 2009, 324, 1697-1699 Y. Inokuma, M. Kawano, M. Fujita, Nat. Chem. 2011, 3, 349-358 S. Horiuchi, T. Murase, M. Fujita, Chem. Asian J. 2011, 6, 1839-1847 C. R. K. Glasson, J. K. Clegg, J. C. McMurtrie, G. V. Meehan, L. F. Lindoy, C. A. Motti, B. Moubaraki, K. S. Murray, J. D. Cashion, Chem. Sci. 2011, 2, 540-543. M. Jung, H. Kim, K. Baek, K. Kim, Angew. Chem. 2008, 120, 5839-5841 J. R. Li, A. A. Yakovenko, W. Lu, D. J. Timmons, W. Zhuang, D. Yuan, H. C. Zhou, J. Am. Chem. Soc. 2010, 132, 17599-17610 I. A. Riddell, M. M. J. Smulders, J. K. Clegg, J. R. Nitschke, Chem. Commun. 2011, 47, 457-459 J. Tranchemontagne, Z. Ni, M. O'Keeffe, O. M. Yaghi, Angew. Chem. 2008, 120, 5214-5225 N. Liédana, A. Galve, C. Rubio, C. Tellez, J. Coronas, ACS Appl. Mater. Interfaces 2012, 4, 5016-5021. J. Bunzen, J. Iwasa, P. Bonakdarzadeh, E. Numata, K. Rissanen, S. Sato, M. Fujita, Angew. Chem. 2012, 124, 3215-3217 Angew. Chem. Int. Ed. 2008, 47, 5136-5147 J. S. Mugridge, A. Zahl, R. V. Eldik, R. G. Bergman, K. N. Raymond, J. Am. Chem. Soc. 2013, 135, 4299-4306 Angew. Chem. Int. Ed. 2013, 52, 4837-4840 D. Zhao, S. Tan, D. Yuan, W. Lu, Y. H. Rezenom, H. Jiang, L.-Q. Wang, H. C. Zhou, Adv. Mater. 2011, 23, 90-93. Angew. Chem. Int. Ed. 2009, 48, 8465-8468 T. Murase, K. Otsuka, M. Fujita, J. Am. Chem. Soc. 2010, 132, 7864-7865 H. Furukawa, J. Kim, N. W. Ockwig, M. O'Keeffe, O. M. Yaghi, J. Am. Chem. Soc. 2008, 130, 11650-11661 J. R. Li, H. C. Zhou, Angew. Chem. 2009, 121, 8617-8620 J. R. Li, H. C. Zhou, Nat. Chem. 2010, 2, 893-898 D. Cunha, M. B. Yahia, S. Hall, S. R. Miller, H. Chevreau, E. Elkaïm, G. Maurin, P. Horcajada, C. Serre, Chem. Mater. 2013, 25, 2767-2776 B. Moulton, J. Lu, A. Mondal, M. J. Zaworotko, Chem. Commun. 2001, 863-864 K. Nakabayashi, Y. Ozaki, M. Kawano, M. Fujita, Angew. Chem. 2008, 120, 2076-2078 T. Murase, H. Takezawa, M. Fujita, Chem. Commun. 2011, 47, 10960-10962 M. Eddaoudi, J. Kim, J. B. Wachter, H. K. Chae, M. O'Keeffe, O. M. Yaghi, J. Am. Chem. Soc. 2001, 123, 4368-4369. P. Horcajada, T. Chalati, C. Serre, B. Gillet, C. Sebrie, T. Baati, J. F. Eubank, D. Heurtaux, P. Clayette, C. Kreuz, J.-S. Chang, Y. K. Hwang, V. Marsaud, P.-N. Bories, L. Cynober, S. Gil, G. Férey, P. Couvreur, R. Gref, Nat. Mater. 2010, 9, 172-178 W. Meng, B. Breiner, K. Rissanen, J. D. Thoburn, J. K. Clegg, J. R. Nitschke, Angew. Chem. 2011, 123, 3541-3545 Q. F. Sun, J. Iwasa, D. Ogawa, Y. Ishido, S. Sato, T. Ozeki, Y. Sei, K. Yamaguchi, M. Fujita, Science 2010, 328, 1144-1147 S. Horiuchi, T. Murase, M. Fujita, J. Am. Chem. Soc. 2011, 133, 12445-12447 T. F. Liu, Y. P. Chen, A. A. Yakovenko, H. C. Zhou, J. Am. Chem. Soc. 2012, 134, 17358-17361. J. K. Clegg, F. Li, K. A. Jolliffe, G. V. Meehan, L. F. Lindoy, Chem. Commun. 2011, 47, 6042-6044 M. Jaya Prakash, M. Oh, X. Liu, K. N. Han, G. H. Seong, M. S. Lah, Chem. Commun. 2010, 46, 2049-2051 J. Park, S. Hong, D. Moon, M. Park, K. Lee, S. Kang, Y. Zou, R. P. John, G. H. Kim, M. S. Lah, Inorg. Chem. 2007, 46, 10208-10213. Angew. Chem. Int. Ed. 2008, 47, 5755-5757 S. Horiuchi, Y. Nishioka, T. Murase, M. Fujita, Chem. Commun. 2010, 46, 3460-3462 S. Sato, Y. Ishido, M. Fujita, J. Am. Chem. Soc. 2009, 131, 6064-6065 C. J. Hastings, M. P. Backlund, R. G. Bergman, K. N. Raymond, Angew. Chem. 2011, 123, 10758-10761 Y. Liu, C. Hu, A. Comotti, M. D. Ward, Science 2011, 333, 436-440 S. Zarra, J. K. Clegg, J. R. Nitschke, Angew. Chem. 2013, 125, 4937-4940 Angew. Chem. Int. Ed. 2011, 50, 10570-10573 Angew. Chem. Int. Ed. 2012, 51, 3161-3163 Angew. Chem. Int. Ed. 2008, 47, 2046-2048 S. Zarra, M. M. J. Smulders, Q. Lefebvre, J. K. Clegg, J. R. Nitschke, Angew. Chem. 2012, 124, 6988-6991 Angew. Chem. Int. Ed. 2012, 51, 6882-6885. M. M. J. Smulders, J. R. Nitschke, Chem. Sci. 2012, 3, 785-788. Angew. Chem. Int. Ed. 2011, 50, 3479-3483 W. Lu, D. Yuan, A. Yakovenko, H.-C. Zhou, Chem. Commun. 2011, 47, 4968-4970. L. B. Sun, J. R. Li, W. Lu, Z. Y. Gu, Z. Luo, H. C. Zhou, J. Am. Chem. Soc. 2012, 134, 15923-15928 2011; 333 2001; 123 2013; 25 2011; 2 2010; 328 2013 2013; 125 52 2011 2011; 123 50 2009; 131 2011; 3 2011; 6 2009 2009; 121 48 2011; 133 2012; 3 2012; 134 2010; 46 2001 2010; 132 2013; 135 2012 2012; 124 51 2011; 23 2011; 47 2010; 2 2012; 4 2008 2008; 120 47 2007; 46 2008; 130 2009; 324 2010; 9 e_1_2_3_4_3 e_1_2_3_4_2 e_1_2_3_16_2 e_1_2_3_37_2 e_1_2_3_2_3 e_1_2_3_16_3 e_1_2_3_2_2 e_1_2_3_18_2 e_1_2_3_39_2 e_1_2_3_8_3 e_1_2_3_33_3 e_1_2_3_8_2 e_1_2_3_12_2 e_1_2_3_33_2 e_1_2_3_6_2 e_1_2_3_14_2 e_1_2_3_35_2 e_1_2_3_10_2 e_1_2_3_31_2 e_1_2_3_26_2 e_1_2_3_28_2 e_1_2_3_28_3 e_1_2_3_22_2 e_1_2_3_45_2 e_1_2_3_24_2 e_1_2_3_41_2 e_1_2_3_20_2 e_1_2_3_43_2 e_1_2_3_19_2 e_1_2_3_1_2 e_1_2_3_5_2 e_1_2_3_15_2 e_1_2_3_38_2 e_1_2_3_15_3 e_1_2_3_3_2 e_1_2_3_17_2 e_1_2_3_9_2 e_1_2_3_11_2 e_1_2_3_34_2 e_1_2_3_7_3 e_1_2_3_7_2 e_1_2_3_13_2 e_1_2_3_36_2 e_1_2_3_30_2 e_1_2_3_32_2 e_1_2_3_9_3 e_1_2_3_27_2 e_1_2_3_29_2 e_1_2_3_23_2 e_1_2_3_44_2 e_1_2_3_25_2 e_1_2_3_40_2 e_1_2_3_21_2 e_1_2_3_42_2 |
| References_xml | – reference: Angew. Chem. Int. Ed. 2012, 51, 6882-6885. – reference: N. Liédana, A. Galve, C. Rubio, C. Tellez, J. Coronas, ACS Appl. Mater. Interfaces 2012, 4, 5016-5021. – reference: K. Nakabayashi, Y. Ozaki, M. Kawano, M. Fujita, Angew. Chem. 2008, 120, 2076-2078; – reference: S. Sato, Y. Ishido, M. Fujita, J. Am. Chem. Soc. 2009, 131, 6064-6065; – reference: Angew. Chem. Int. Ed. 2011, 50, 10570-10573; – reference: L. B. Sun, J. R. Li, W. Lu, Z. Y. Gu, Z. Luo, H. C. Zhou, J. Am. Chem. Soc. 2012, 134, 15923-15928; – reference: Y. Inokuma, M. Kawano, M. Fujita, Nat. Chem. 2011, 3, 349-358; – reference: J. S. Mugridge, A. Zahl, R. V. Eldik, R. G. Bergman, K. N. Raymond, J. Am. Chem. Soc. 2013, 135, 4299-4306; – reference: T. F. Liu, Y. P. Chen, A. A. Yakovenko, H. C. Zhou, J. Am. Chem. Soc. 2012, 134, 17358-17361. – reference: Angew. Chem. Int. Ed. 2012, 51, 3161-3163; – reference: H. Furukawa, J. Kim, N. W. Ockwig, M. O'Keeffe, O. M. Yaghi, J. Am. Chem. Soc. 2008, 130, 11650-11661; – reference: J. Tranchemontagne, Z. Ni, M. O'Keeffe, O. M. Yaghi, Angew. Chem. 2008, 120, 5214-5225; – reference: S. Zarra, J. K. Clegg, J. R. Nitschke, Angew. Chem. 2013, 125, 4937-4940; – reference: T. Murase, H. Takezawa, M. Fujita, Chem. Commun. 2011, 47, 10960-10962; – reference: W. Lu, D. Yuan, A. Yakovenko, H.-C. Zhou, Chem. Commun. 2011, 47, 4968-4970. – reference: J. Bunzen, J. Iwasa, P. Bonakdarzadeh, E. Numata, K. Rissanen, S. Sato, M. Fujita, Angew. Chem. 2012, 124, 3215-3217; – reference: Angew. Chem. Int. Ed. 2008, 47, 5755-5757; – reference: J. R. Li, H. C. Zhou, Angew. Chem. 2009, 121, 8617-8620; – reference: D. Cunha, M. B. Yahia, S. Hall, S. R. Miller, H. Chevreau, E. Elkaïm, G. Maurin, P. Horcajada, C. Serre, Chem. Mater. 2013, 25, 2767-2776; – reference: Angew. Chem. Int. Ed. 2008, 47, 2046-2048; – reference: W. Meng, B. Breiner, K. Rissanen, J. D. Thoburn, J. K. Clegg, J. R. Nitschke, Angew. Chem. 2011, 123, 3541-3545; – reference: Angew. Chem. Int. Ed. 2008, 47, 5136-5147; – reference: Y. Liu, C. Hu, A. Comotti, M. D. Ward, Science 2011, 333, 436-440; – reference: J. K. Clegg, F. Li, K. A. Jolliffe, G. V. Meehan, L. F. Lindoy, Chem. Commun. 2011, 47, 6042-6044; – reference: J. R. Li, A. A. Yakovenko, W. Lu, D. J. Timmons, W. Zhuang, D. Yuan, H. C. Zhou, J. Am. Chem. Soc. 2010, 132, 17599-17610; – reference: S. Zarra, M. M. J. Smulders, Q. Lefebvre, J. K. Clegg, J. R. Nitschke, Angew. Chem. 2012, 124, 6988-6991; – reference: C. J. Hastings, M. P. Backlund, R. G. Bergman, K. N. Raymond, Angew. Chem. 2011, 123, 10758-10761; – reference: Q. F. Sun, J. Iwasa, D. Ogawa, Y. Ishido, S. Sato, T. Ozeki, Y. Sei, K. Yamaguchi, M. Fujita, Science 2010, 328, 1144-1147; – reference: S. Horiuchi, T. Murase, M. Fujita, Chem. Asian J. 2011, 6, 1839-1847; – reference: Angew. Chem. Int. Ed. 2013, 52, 4837-4840; – reference: J. Park, S. Hong, D. Moon, M. Park, K. Lee, S. Kang, Y. Zou, R. P. John, G. H. Kim, M. S. Lah, Inorg. Chem. 2007, 46, 10208-10213. – reference: D. Zhao, S. Tan, D. Yuan, W. Lu, Y. H. Rezenom, H. Jiang, L.-Q. Wang, H. C. Zhou, Adv. Mater. 2011, 23, 90-93. – reference: J. R. Li, H. C. Zhou, Nat. Chem. 2010, 2, 893-898; – reference: Angew. Chem. Int. Ed. 2011, 50, 3479-3483; – reference: P. Mal, B. Breiner, K. Rissanen, J. R. Nitschke, Science 2009, 324, 1697-1699; – reference: M. Jaya Prakash, M. Oh, X. Liu, K. N. Han, G. H. Seong, M. S. Lah, Chem. Commun. 2010, 46, 2049-2051; – reference: B. Moulton, J. Lu, A. Mondal, M. J. Zaworotko, Chem. Commun. 2001, 863-864; – reference: C. R. K. Glasson, J. K. Clegg, J. C. McMurtrie, G. V. Meehan, L. F. Lindoy, C. A. Motti, B. Moubaraki, K. S. Murray, J. D. Cashion, Chem. Sci. 2011, 2, 540-543. – reference: P. Horcajada, T. Chalati, C. Serre, B. Gillet, C. Sebrie, T. Baati, J. F. Eubank, D. Heurtaux, P. Clayette, C. Kreuz, J.-S. Chang, Y. K. Hwang, V. Marsaud, P.-N. Bories, L. Cynober, S. Gil, G. Férey, P. Couvreur, R. Gref, Nat. Mater. 2010, 9, 172-178; – reference: S. Horiuchi, T. Murase, M. Fujita, J. Am. Chem. Soc. 2011, 133, 12445-12447; – reference: M. Eddaoudi, J. Kim, J. B. Wachter, H. K. Chae, M. O'Keeffe, O. M. Yaghi, J. Am. Chem. Soc. 2001, 123, 4368-4369. – reference: M. Jung, H. Kim, K. Baek, K. Kim, Angew. Chem. 2008, 120, 5839-5841; – reference: M. M. J. Smulders, J. R. Nitschke, Chem. Sci. 2012, 3, 785-788. – reference: T. Murase, K. Otsuka, M. Fujita, J. Am. Chem. Soc. 2010, 132, 7864-7865; – reference: Angew. Chem. Int. Ed. 2009, 48, 8465-8468; – reference: I. A. Riddell, M. M. J. Smulders, J. K. Clegg, J. R. Nitschke, Chem. Commun. 2011, 47, 457-459; – reference: S. Horiuchi, Y. Nishioka, T. Murase, M. Fujita, Chem. Commun. 2010, 46, 3460-3462; – volume: 46 start-page: 10208 year: 2007 end-page: 10213 publication-title: Inorg. Chem. – volume: 132 start-page: 7864 year: 2010 end-page: 7865 publication-title: J. Am. Chem. Soc. – volume: 123 start-page: 4368 year: 2001 end-page: 4369 publication-title: J. Am. Chem. Soc. – volume: 134 start-page: 15923 year: 2012 end-page: 15928 publication-title: J. Am. Chem. Soc. – volume: 121 48 start-page: 8617 8465 year: 2009 2009 end-page: 8620 8468 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 131 start-page: 6064 year: 2009 end-page: 6065 publication-title: J. Am. Chem. Soc. – volume: 4 start-page: 5016 year: 2012 end-page: 5021 publication-title: ACS Appl. Mater. Interfaces – start-page: 863 year: 2001 end-page: 864 publication-title: Chem. Commun. – volume: 120 47 start-page: 2076 2046 year: 2008 2008 end-page: 2078 2048 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 46 start-page: 3460 year: 2010 end-page: 3462 publication-title: Chem. Commun. – volume: 133 start-page: 12445 year: 2011 end-page: 12447 publication-title: J. Am. Chem. Soc. – volume: 47 start-page: 6042 year: 2011 end-page: 6044 publication-title: Chem. Commun. – volume: 135 start-page: 4299 year: 2013 end-page: 4306 publication-title: J. Am. Chem. Soc. – volume: 47 start-page: 457 year: 2011 end-page: 459 publication-title: Chem. Commun. – volume: 333 start-page: 436 year: 2011 end-page: 440 publication-title: Science – volume: 125 52 start-page: 4937 4837 year: 2013 2013 end-page: 4940 4840 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 9 start-page: 172 year: 2010 end-page: 178 publication-title: Nat. Mater. – volume: 47 start-page: 10960 year: 2011 end-page: 10962 publication-title: Chem. Commun. – volume: 46 start-page: 2049 year: 2010 end-page: 2051 publication-title: Chem. Commun. – volume: 130 start-page: 11650 year: 2008 end-page: 11661 publication-title: J. Am. Chem. Soc. – volume: 132 start-page: 17599 year: 2010 end-page: 17610 publication-title: J. Am. Chem. Soc. – volume: 120 47 start-page: 5214 5136 year: 2008 2008 end-page: 5225 5147 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 324 start-page: 1697 year: 2009 end-page: 1699 publication-title: Science – volume: 3 start-page: 349 year: 2011 end-page: 358 publication-title: Nat. Chem. – volume: 120 47 start-page: 5839 5755 year: 2008 2008 end-page: 5841 5757 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 123 50 start-page: 3541 3479 year: 2011 2011 end-page: 3545 3483 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 124 51 start-page: 3215 3161 year: 2012 2012 end-page: 3217 3163 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 123 50 start-page: 10758 10570 year: 2011 2011 end-page: 10761 10573 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 134 start-page: 17358 year: 2012 end-page: 17361 publication-title: J. Am. Chem. Soc. – volume: 3 start-page: 785 year: 2012 end-page: 788 publication-title: Chem. Sci. – volume: 6 start-page: 1839 year: 2011 end-page: 1847 publication-title: Chem. Asian J. – volume: 2 start-page: 540 year: 2011 end-page: 543 publication-title: Chem. Sci. – volume: 25 start-page: 2767 year: 2013 end-page: 2776 publication-title: Chem. Mater. – volume: 23 start-page: 90 year: 2011 end-page: 93 publication-title: Adv. Mater. – volume: 328 start-page: 1144 year: 2010 end-page: 1147 publication-title: Science – volume: 2 start-page: 893 year: 2010 end-page: 898 publication-title: Nat. Chem. – volume: 47 start-page: 4968 year: 2011 end-page: 4970 publication-title: Chem. Commun. – volume: 124 51 start-page: 6988 6882 year: 2012 2012 end-page: 6991 6885 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – ident: e_1_2_3_16_2 doi: 10.1002/ange.200802240 – ident: e_1_2_3_7_2 doi: 10.1002/ange.201100193 – ident: e_1_2_3_45_2 doi: 10.1021/am301365h – ident: e_1_2_3_25_2 doi: 10.1039/c1cc14523a – ident: e_1_2_3_28_3 doi: 10.1002/anie.201105325 – ident: e_1_2_3_21_2 doi: 10.1039/C0CC02573A – ident: e_1_2_3_15_3 doi: 10.1002/anie.200704924 – ident: e_1_2_3_40_2 doi: 10.1021/ja306150x – ident: e_1_2_3_30_2 doi: 10.1039/c1cc11167a – ident: e_1_2_3_14_2 doi: 10.1021/ja803783c – ident: e_1_2_3_10_2 – ident: e_1_2_3_7_3 doi: 10.1002/anie.201100193 – ident: e_1_2_3_34_2 doi: 10.1038/nchem.803 – ident: e_1_2_3_28_2 doi: 10.1002/ange.201105325 – ident: e_1_2_3_36_2 doi: 10.1039/c1cc00030f – ident: e_1_2_3_15_2 doi: 10.1002/ange.200704924 – ident: e_1_2_3_11_2 doi: 10.1039/b102714j – ident: e_1_2_3_22_2 doi: 10.1039/C1SC00847A – ident: e_1_2_3_32_2 – ident: e_1_2_3_16_3 doi: 10.1002/anie.200802240 – ident: e_1_2_3_1_2 – ident: e_1_2_3_23_2 – ident: e_1_2_3_17_2 doi: 10.1021/ja103109z – ident: e_1_2_3_42_2 – ident: e_1_2_3_44_2 doi: 10.1021/cm400798p – ident: e_1_2_3_33_3 doi: 10.1002/anie.201209694 – ident: e_1_2_3_37_2 doi: 10.1002/adma.201003012 – ident: e_1_2_3_8_3 doi: 10.1002/anie.201108731 – ident: e_1_2_3_19_2 doi: 10.1021/ja205450a – ident: e_1_2_3_9_2 doi: 10.1002/ange.201202665 – ident: e_1_2_3_4_2 doi: 10.1002/ange.200904722 – ident: e_1_2_3_29_2 doi: 10.1126/science.1204369 – ident: e_1_2_3_3_2 doi: 10.1126/science.1175313 – ident: e_1_2_3_2_2 doi: 10.1002/ange.200705008 – ident: e_1_2_3_33_2 doi: 10.1002/ange.201209694 – ident: e_1_2_3_4_3 doi: 10.1002/anie.200904722 – ident: e_1_2_3_12_2 doi: 10.1021/ic7013623 – ident: e_1_2_3_39_2 doi: 10.1021/ja3063925 – ident: e_1_2_3_18_2 doi: 10.1021/ja1080794 – ident: e_1_2_3_13_2 – ident: e_1_2_3_2_3 doi: 10.1002/anie.200705008 – ident: e_1_2_3_9_3 doi: 10.1002/anie.201202665 – ident: e_1_2_3_20_2 doi: 10.1038/nchem.1031 – ident: e_1_2_3_26_2 doi: 10.1002/asia.201000842 – ident: e_1_2_3_31_2 doi: 10.1039/C0SC00523A – ident: e_1_2_3_41_2 doi: 10.1021/ja0104352 – ident: e_1_2_3_35_2 doi: 10.1021/ja900676f – ident: e_1_2_3_38_2 – ident: e_1_2_3_5_2 doi: 10.1039/b925335a – ident: e_1_2_3_43_2 doi: 10.1038/nmat2608 – ident: e_1_2_3_27_2 doi: 10.1021/ja309949q – ident: e_1_2_3_6_2 doi: 10.1126/science.1188605 – ident: e_1_2_3_8_2 doi: 10.1002/ange.201108731 – ident: e_1_2_3_24_2 doi: 10.1039/c003191g |
| SSID | ssj0028806 |
| Score | 2.3949842 |
| Snippet | Twist and release: The metal–organic polyhedron 1 synthesized from 5‐(prop‐2‐ynyloxy)isophthalic acid and Cu(NO3)2⋅ 3 H2O has a hydrophobic outer surface and a... Twist and release: The metal-organic polyhedron 1 synthesized from 5-(prop-2-ynyloxy)isophthalic acid and Cu(NO3 )2 ⋅ 3 H2 O has a hydrophobic outer surface... Twist and release: The metal-organic polyhedron 1 synthesized from 5-(prop-2-ynyloxy)isophthalic acid and Cu(NO3 )2 3H2 O has a hydrophobic outer surface and a... Twist and release: The metal-organic polyhedron 1 synthesized from 5-(prop-2-ynyloxy)isophthalic acid and Cu(NO sub(3)) sub(2) 3H sub(2)O has a hydrophobic... |
| SourceID | proquest pubmed crossref wiley istex |
| SourceType | Aggregation Database Index Database Enrichment Source Publisher |
| StartPage | 13755 |
| SubjectTerms | cage compounds Conversion crystal engineering Drugs hydrophobic effect Metal-organic frameworks Metals Polarity Polyhedrons self-assembly Transformations Two dimensional |
| Title | Hydrolytic Conversion of a Metal-Organic Polyhedron into a Metal-Organic Framework |
| URI | https://api.istex.fr/ark:/67375/WNG-GTTTHTBW-S/fulltext.pdf https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.201307486 https://www.ncbi.nlm.nih.gov/pubmed/24346950 https://www.proquest.com/docview/1468610004 https://www.proquest.com/docview/1469639125 https://www.proquest.com/docview/1701123527 |
| Volume | 52 |
| hasFullText | 1 |
| inHoldings | 1 |
| isFullTextHit | |
| isPrint | |
| link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9QwEB5V5VAuvMojpaAgITilTbx2Hsey6nZbqasKUtqb5adArZJquytRTvyH_sP-EmaSTWBRAQluiTyOYs_Y_mzPfAPwWsWFx4UoidI89hG3SkQFTooI5HiiCyMQotN5x-EkHR_zg1Nx-lMUf8sP0R-40cho5msa4Epfbv8gDaUIbHLNQiPlOXFuk8MWoaL3PX8UQ-Nsw4sGg4iy0HesjTHbXq6-tCrdoQ7-chvkXEawzRI0ug-q-_nW8-Rsaz7TW-brL7yO_9O6B3BvgU_DndagHsKKqx7B2rBLC7cOH8dXdlqfX2F5OCSX9ea8Lax9qMJDh1D-5tt1G-BpwiOU--RQvAo_V7P6FolR5xv2GI5Hu-VwHC2SM0SG50kacce1G2SZKryLubfO5M6z2NjEk4a55tYJ41mhhEm95im3Od3i6kIr4XH7-wRWq7pyzyAUMbOxsxSCm3BrdW4pKVOiLPO4GfNJAFGnHGkWzOWUQONctpzLTFJvyb63Anjby1-0nB2_lXzT6LoXU9Mz8nTLhDyZ7Mm9sizH5bsT-SGAzc4Y5GKQX9KuKU_pfoQH8KovRnXQnYuqXD1vZHCKKxBG_kEmw0mWIRLOAnjaGlr_Q4wP8AsiDoA15vKXBsmdyf5u_7bxL5Wew116JpedJN2E1dl07l4g8Jrpl83g-g65jyTa |
| linkProvider | Wiley-Blackwell |
| linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9QwEB5BeyiXlmdJKRAkBKe0idfO41hW3abQXSFIKTfLjm1RtUrQsitRTvyH_sP-EmaSTdCiAhIcE4-j2J4Zf2PPA-C5CjOHG1EUxGnoAm6UCDJUigjkeKSzUiBEp_OO8STOj_nrj6LzJqRYmDY_RH_gRpLR6GsScDqQ3v2ZNZRCsMk3C7mUp_FNWKWy3o1V9a7PIMWQPdsAo8EgoDr0Xd7GkO0u91_al1Zpir9eBzqXMWyzCY02QHe_3_qenO3MZ3qn_PZLZsf_Gt9tWF9AVH-v5ak7cMNWd2Ft2FWGuwcf8gszrc8vsN0fktd6c-Tm185X_tgimr_6ftnGeJb-W6T7ZJG88k-rWX0NxahzD7sPx6P9YpgHi_oMQcnTKA645doOkkRlzobcGVum1rGwNJGjReaaGytKxzIlythpHnOT0kWuzrQSDi3gB7BS1ZV9CL4ImQmtoSjciBujU0N1mSJlmEN7zEUeBN3qyHKRvJxqaJzLNu0ykzRbsp8tD1729J_btB2_pXzRLHZPpqZn5OyWCHkyOZAHRVHkxasT-d6D7Y4b5ELOv5DhlMZ0RcI9eNY343LQtYuqbD1vaFDLZYgk_0CToJ5lCIYTDzZbTut_iPEBfkGEHrCGX_4yILk3Odzvn7b-pdNTWMuL8ZE8Opy8eQS36D158ETxNqzMpnP7GHHYTD9pJO0H9O8o9Q |
| linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9QwEB5BKwEX3o9AgSAhOKVNvLaTHMu22y3QVQUp7c1y_BCoVVItuxLlxH_gH_JLmEk2gUUFJDgmHkex5-HP9jwAnuo497gQJZHMYh9xq0WUo1FEIMeTMjcCITqdd-xN5PiAvzwSRz9F8bf5IfoDN9KMxl6Tgp9av_EjaShFYJNrFgopz-RFWOUyzkiut970CaQYSmcbXzQYRFSGvkvbGLON5f5Ly9IqzfCn8zDnMoRt1qDRNdDd37euJ8fr81m5bj7_ktjxf4Z3Ha4uAGq42UrUDbjgqptwedjVhbsF78ZndlqfnGF7OCSf9ebALax9qMM9h1j-25evbYSnCfeR7r1D8ir8UM3qcyhGnXPYbTgYbRfDcbSozhAZniUy4o6XbpCmOvcu5t46kznPYmMTTyzmJbdOGM9yLYz0JZfcZnSNW-alFh73v3dgpaordw9CETMbO0sxuAm3tswsVWVKtGUed2M-CSDqmKPMInU5VdA4UW3SZaZotlQ_WwE87-lP26Qdv6V81vC6J9PTY3J1S4U6nOyonaIoxsWLQ_U2gLVOGNRCyz_StimTdEHCA3jSNyM76NJFV66eNzRo43LEkX-gSdHKMoTCaQB3W0Hrf4jxAX5BxAGwRlz-MiC1Odnd7p_u_0unx3Bpf2ukXu9OXj2AK_Sa3HcSuQYrs-ncPUQQNisfNXr2HXRqJ60 |
| 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=Hydrolytic+conversion+of+a+metal-organic+polyhedron+into+a+metal-organic+framework&rft.jtitle=Angewandte+Chemie+International+Edition&rft.au=Mallick%2C+Arijit&rft.au=Garai%2C+Bikash&rft.au=D%C3%ADaz%2C+David+D%C3%ADaz&rft.au=Banerjee%2C+Rahul&rft.date=2013-12-16&rft.issn=1521-3773&rft.eissn=1521-3773&rft.volume=52&rft.issue=51&rft.spage=13755&rft_id=info:doi/10.1002%2Fanie.201307486&rft.externalDBID=NO_FULL_TEXT |
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1433-7851&client=summon |
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1433-7851&client=summon |
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1433-7851&client=summon |