Color- and Morphology-Controlled Self-Assembly of New Electron-Donor-Substituted Aggregation-Induced Emission Compounds
Four electron-donor-substituted aggregation-induced emission (AIE) compounds, N,N′-bis(4-methoxylsalicylidene)-p-phenylenediamine (BSPD-OMe), N,N′-bis(4-methylsalicylidene)-p-phenylenediamine (BSPD-Me), N,N′-bis(salicylidene)-p-phenylenediamine (BSPD), and N,N′-bis(4-hydroxylsalicylidene)-p-phenylen...
Saved in:
Published in | Langmuir Vol. 30; no. 9; pp. 2351 - 2359 |
---|---|
Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Chemical Society
11.03.2014
|
Online Access | Get full text |
Cover
Loading…
Abstract | Four electron-donor-substituted aggregation-induced emission (AIE) compounds, N,N′-bis(4-methoxylsalicylidene)-p-phenylenediamine (BSPD-OMe), N,N′-bis(4-methylsalicylidene)-p-phenylenediamine (BSPD-Me), N,N′-bis(salicylidene)-p-phenylenediamine (BSPD), and N,N′-bis(4-hydroxylsalicylidene)-p-phenylenediamine (BSPD-OH), are designed and synthesized. They are all found to exhibit controlled self-assembly behaviors and good thermal properties. By changing the terminal electron-donor groups, they are controlled to self-assemble into three emission colors (green, yellow, and orange) and four morphologies (microblocks, microparticles, microrods, and nanowires) in THF/water mixtures. Their self-assembled structures were investigated with scanning electron microscopy (SEM), fluorescent microscopy images, transmission electron microscopy (TEM), and powder X-ray diffraction (PXRD) techniques. In addition, the emission colors of BSPD-OH can be successfully controlled to three colors (green → yellow → orange) through simply changing the water fraction (f w). Their thermal gravimetric analysis (TGA) results indicate that their thermal decomposition temperatures (T d, corresponding to 5% weight loss) range from 282 to 319 °C. Their differential scanning calorimetry (DSC) data show that BSPD-OH bears a glass-transition temperature (T g) of 118 °C. The good T d and T g values will ensure them to be luminogens for organic light-emitting diodes (OLEDs). The theoretical calculations and single-crystal X-ray diffraction (XRD) analysis of BSPD-OMe and BSPD suggest that the stronger electron donor substituent can twist the molecular conformation, decrease the degree of π conjugation, increase the energy gap, and then induce the emission colors’ blue shift and morphology variation. The results are meaningful in controlling the emission colors and self-assembly shapes of these derivatives, and they also provide a novel but facile way to get color-tunable AIE luminogens for OLEDs. |
---|---|
AbstractList | Four electron-donor-substituted aggregation-induced emission (AIE) compounds, N,N'-bis(4-methoxylsalicylidene)-p-phenylenediamine (BSPD-OMe), N,N'-bis(4-methylsalicylidene)-p-phenylenediamine (BSPD-Me), N,N'-bis(salicylidene)-p-phenylenediamine (BSPD), and N,N'-bis(4-hydroxylsalicylidene)-p-phenylenediamine (BSPD-OH), are designed and synthesized. They are all found to exhibit controlled self-assembly behaviors and good thermal properties. By changing the terminal electron-donor groups, they are controlled to self-assemble into three emission colors (green, yellow, and orange) and four morphologies (microblocks, microparticles, microrods, and nanowires) in THF/water mixtures. Their self-assembled structures were investigated with scanning electron microscopy (SEM), fluorescent microscopy images, transmission electron microscopy (TEM), and powder X-ray diffraction (PXRD) techniques. In addition, the emission colors of BSPD-OH can be successfully controlled to three colors (green → yellow → orange) through simply changing the water fraction (fw). Their thermal gravimetric analysis (TGA) results indicate that their thermal decomposition temperatures (Td, corresponding to 5% weight loss) range from 282 to 319 °C. Their differential scanning calorimetry (DSC) data show that BSPD-OH bears a glass-transition temperature (Tg) of 118 °C. The good Td and Tg values will ensure them to be luminogens for organic light-emitting diodes (OLEDs). The theoretical calculations and single-crystal X-ray diffraction (XRD) analysis of BSPD-OMe and BSPD suggest that the stronger electron donor substituent can twist the molecular conformation, decrease the degree of π conjugation, increase the energy gap, and then induce the emission colors' blue shift and morphology variation. The results are meaningful in controlling the emission colors and self-assembly shapes of these derivatives, and they also provide a novel but facile way to get color-tunable AIE luminogens for OLEDs. Four electron-donor-substituted aggregation-induced emission (AIE) compounds, N,N′-bis(4-methoxylsalicylidene)-p-phenylenediamine (BSPD-OMe), N,N′-bis(4-methylsalicylidene)-p-phenylenediamine (BSPD-Me), N,N′-bis(salicylidene)-p-phenylenediamine (BSPD), and N,N′-bis(4-hydroxylsalicylidene)-p-phenylenediamine (BSPD-OH), are designed and synthesized. They are all found to exhibit controlled self-assembly behaviors and good thermal properties. By changing the terminal electron-donor groups, they are controlled to self-assemble into three emission colors (green, yellow, and orange) and four morphologies (microblocks, microparticles, microrods, and nanowires) in THF/water mixtures. Their self-assembled structures were investigated with scanning electron microscopy (SEM), fluorescent microscopy images, transmission electron microscopy (TEM), and powder X-ray diffraction (PXRD) techniques. In addition, the emission colors of BSPD-OH can be successfully controlled to three colors (green → yellow → orange) through simply changing the water fraction (f w). Their thermal gravimetric analysis (TGA) results indicate that their thermal decomposition temperatures (T d, corresponding to 5% weight loss) range from 282 to 319 °C. Their differential scanning calorimetry (DSC) data show that BSPD-OH bears a glass-transition temperature (T g) of 118 °C. The good T d and T g values will ensure them to be luminogens for organic light-emitting diodes (OLEDs). The theoretical calculations and single-crystal X-ray diffraction (XRD) analysis of BSPD-OMe and BSPD suggest that the stronger electron donor substituent can twist the molecular conformation, decrease the degree of π conjugation, increase the energy gap, and then induce the emission colors’ blue shift and morphology variation. The results are meaningful in controlling the emission colors and self-assembly shapes of these derivatives, and they also provide a novel but facile way to get color-tunable AIE luminogens for OLEDs. |
Author | Zhao, Liu Ma, Hui Han, Jingsa Deng, Xuebin Zhang, Jiaxin Fang, Tao Ouyang, Jin Niu, Caixia Na, Na |
AuthorAffiliation | Key Laboratory of Theoretical and Computational Photochemistry, Ministry of Education, College of Chemistry Beijing Normal University Analytical and Testing Center |
AuthorAffiliation_xml | – name: Beijing Normal University – name: – name: Key Laboratory of Theoretical and Computational Photochemistry, Ministry of Education, College of Chemistry – name: Analytical and Testing Center |
Author_xml | – sequence: 1 givenname: Caixia surname: Niu fullname: Niu, Caixia – sequence: 2 givenname: Liu surname: Zhao fullname: Zhao, Liu – sequence: 3 givenname: Tao surname: Fang fullname: Fang, Tao – sequence: 4 givenname: Xuebin surname: Deng fullname: Deng, Xuebin – sequence: 5 givenname: Hui surname: Ma fullname: Ma, Hui – sequence: 6 givenname: Jiaxin surname: Zhang fullname: Zhang, Jiaxin – sequence: 7 givenname: Na surname: Na fullname: Na, Na – sequence: 8 givenname: Jingsa surname: Han fullname: Han, Jingsa – sequence: 9 givenname: Jin surname: Ouyang fullname: Ouyang, Jin email: jinoyang@bnu.edu.cn |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24571508$$D View this record in MEDLINE/PubMed |
BookMark | eNptkD9PwzAQxS1UBC0w8AVQFiQYDI7jxPVYhQKV-DMU5siOL6WVYxc7oeq3x6jQiel0d797uvdGaGCdBYTOU3KTEpreGskIY1nxdYCGaU4JzseUD9CQcJZhzorsGI1CWBFCRMbEETqmLOdpTsZDtCmdcR4n0urk2fn1R2wXW1w623lnDOhkDqbBkxCgVWabuCZ5gU0yNVBHwOI7Z-P5vFehW3Z9F_nJYuFhIbtl3M6s7us4m7bLEOIgKV27dr3V4RQdNtIEOPutJ-j9fvpWPuKn14dZOXnCMhunHdZaFDwToCQVGVVqLIqcFtAUAqSi0WqtSc2BkVpQTfNCc6aUBtA5NMDizQm62umuvfvsIXRVfKUGY6QF14cqplBwkTKeRfR6h9beheChqdZ-2Uq_rVJS_eRc7XOO7MWvbK9a0HvyL9gIXO4AWYdq5Xpvo8t_hL4BHACILw |
CitedBy_id | crossref_primary_10_1021_jp510476h crossref_primary_10_1002_chem_201501902 crossref_primary_10_3390_ijms232012439 crossref_primary_10_1016_j_cclet_2018_05_043 crossref_primary_10_1039_C4RA10021B crossref_primary_10_1016_j_aca_2016_09_036 crossref_primary_10_1007_s12161_019_01521_8 crossref_primary_10_1002_adfm_201807211 crossref_primary_10_1016_j_saa_2018_07_021 crossref_primary_10_1007_s00396_016_3896_5 crossref_primary_10_1016_j_jlumin_2018_08_014 crossref_primary_10_1021_jp5068439 crossref_primary_10_3390_molecules25143298 crossref_primary_10_1039_C9TC00143C crossref_primary_10_1039_C4OB01058B crossref_primary_10_1039_C5RA17570D crossref_primary_10_1007_s10895_015_1717_8 crossref_primary_10_3390_app7111119 crossref_primary_10_1039_C4TC02726D crossref_primary_10_1080_00958972_2021_1897114 crossref_primary_10_1038_srep19277 crossref_primary_10_1039_C5NJ01052G crossref_primary_10_1039_C7CE01872J crossref_primary_10_1016_j_dyepig_2022_110330 crossref_primary_10_1016_j_saa_2021_120433 crossref_primary_10_1039_C6FD00171H crossref_primary_10_1016_j_jphotochem_2017_11_044 crossref_primary_10_1039_C9NJ03297E crossref_primary_10_1002_cptc_202000099 crossref_primary_10_1016_j_molstruc_2022_132399 crossref_primary_10_1021_jacs_5b11497 crossref_primary_10_1016_j_molliq_2019_112262 crossref_primary_10_1016_j_jtice_2017_03_023 crossref_primary_10_1039_C5RA04228C crossref_primary_10_1002_slct_201800158 crossref_primary_10_1039_C6RA16244D crossref_primary_10_1007_s11237_018_9558_6 crossref_primary_10_3390_sym15020424 crossref_primary_10_1002_adsc_202300528 crossref_primary_10_1002_chem_201604315 crossref_primary_10_1016_j_jcis_2022_05_021 crossref_primary_10_1016_j_polymer_2023_125703 crossref_primary_10_1016_j_snb_2018_02_126 crossref_primary_10_12677_HJMCe_2019_73006 crossref_primary_10_1016_j_snb_2017_11_127 crossref_primary_10_1039_C5NR00554J crossref_primary_10_1016_j_dyepig_2016_11_048 crossref_primary_10_1021_acs_jcim_0c01430 crossref_primary_10_1016_j_ica_2019_03_034 crossref_primary_10_1021_acs_langmuir_6b04301 crossref_primary_10_1039_c6pp00122j crossref_primary_10_1002_chem_202000526 crossref_primary_10_1016_j_saa_2021_119515 crossref_primary_10_1021_acs_cgd_7b00351 crossref_primary_10_1039_C5CS00543D crossref_primary_10_1021_acs_langmuir_5b00155 crossref_primary_10_1002_asia_201801884 crossref_primary_10_1021_acs_chemrev_5b00263 |
Cites_doi | 10.1021/ja0680257 10.1039/b105159h 10.1021/ja400337p 10.1039/c1jm12098k 10.1021/jp0488012 10.1021/la202755z 10.1021/ol801855s 10.1021/cr030070z 10.1021/cr0501339 10.1039/C2TA00574C 10.1038/35001541 10.1021/ja050168q 10.1126/science.1070821 10.1002/smll.201002195 10.1021/jp407623u 10.1021/jo802631m 10.1039/c2cc33172a 10.1351/PAC-CON-13-02-06 10.1021/ma000100p 10.1021/jp973225d 10.1021/ja806162h 10.1021/la104302d 10.1039/c1cp21039d 10.1021/ja1027502 10.1002/adma.201102804 10.1021/la904727t 10.1002/adma.201101059 |
ContentType | Journal Article |
Copyright | Copyright © 2014 American
Chemical Society |
Copyright_xml | – notice: Copyright © 2014 American Chemical Society |
DBID | NPM AAYXX CITATION 7X8 |
DOI | 10.1021/la404436v |
DatabaseName | PubMed CrossRef MEDLINE - Academic |
DatabaseTitle | PubMed CrossRef MEDLINE - Academic |
DatabaseTitleList | PubMed MEDLINE - Academic |
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 | 1520-5827 |
EndPage | 2359 |
ExternalDocumentID | 10_1021_la404436v 24571508 a709993380 |
Genre | Journal Article |
GroupedDBID | - .K2 02 4.4 53G 55A 5GY 5VS 7~N AABXI ABFLS ABMVS ABPTK ABUCX ACGFS ACJ ACNCT ACS AEESW AENEX AFEFF ALMA_UNASSIGNED_HOLDINGS AQSVZ BAANH CS3 DU5 EBS ED ED~ EJD F5P GNL IH9 IHE JG JG~ K2 LG6 RNS ROL TN5 UI2 UPT VF5 VG9 W1F X --- -~X AAHBH ABJNI ABQRX ADHLV AGXLV AHGAQ CUPRZ GGK NPM YQT ~02 AAYXX CITATION 7X8 |
ID | FETCH-LOGICAL-a381t-dd96739eba2932bb896526ef69eab2520cd0c7e40c92d256d74bbdeed5efe4293 |
IEDL.DBID | ACS |
ISSN | 0743-7463 |
IngestDate | Fri Aug 16 14:55:51 EDT 2024 Fri Aug 23 01:16:43 EDT 2024 Sat Sep 28 08:02:41 EDT 2024 Thu Aug 27 13:42:25 EDT 2020 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 9 |
Language | English |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-a381t-dd96739eba2932bb896526ef69eab2520cd0c7e40c92d256d74bbdeed5efe4293 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
PMID | 24571508 |
PQID | 1506791473 |
PQPubID | 23479 |
PageCount | 9 |
ParticipantIDs | proquest_miscellaneous_1506791473 crossref_primary_10_1021_la404436v pubmed_primary_24571508 acs_journals_10_1021_la404436v |
ProviderPackageCode | JG~ 55A AABXI GNL VF5 7~N ACJ VG9 W1F ACS AEESW AFEFF .K2 ABMVS ABUCX IH9 BAANH AQSVZ ED~ UI2 |
PublicationCentury | 2000 |
PublicationDate | 2014-03-11 |
PublicationDateYYYYMMDD | 2014-03-11 |
PublicationDate_xml | – month: 03 year: 2014 text: 2014-03-11 day: 11 |
PublicationDecade | 2010 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States |
PublicationTitle | Langmuir |
PublicationTitleAlternate | Langmuir |
PublicationYear | 2014 |
Publisher | American Chemical Society |
Publisher_xml | – name: American Chemical Society |
References | Yang G. Q. (ref21/cit21) 2013; 85 Chahine J. (ref27/cit27) 2011; 27 Oelkrug D. (ref28/cit28) 1998; 102 Li C. (ref3/cit3) 2005; 127 Randino C. (ref24/cit24) 2011; 13 An B. K. (ref25/cit25) 2009; 131 Whitesides G. M. (ref2/cit2) 2002; 295 Li S. Y. (ref23/cit23) 2004; 108 Chen S. J. (ref13/cit13) 2013; 135 Song P. S. (ref19/cit19) 2011; 21 Luo X. L. (ref16/cit16) 2011; 23 Gu X. G. (ref17/cit17) 2012; 22 Thomas S. W. (ref8/cit8) 2007; 107 Chen X. L. (ref5/cit5) 2000; 33 Shellaiah M. (ref20/cit20) 2013; 1 Kim S. (ref6/cit6) 2007; 129 Yan Q. (ref4/cit4) 2010; 132 Zhao Z. J. (ref14/cit14) 2011; 23 Lu H. G. (ref15/cit15) 2010; 26 Luo J. D. (ref9/cit9) 2001 Hoeben F. J. M. (ref1/cit1) 2005; 105 Tang W. X. (ref18/cit18) 2009; 74 Javed I. (ref26/cit26) 2012; 28 Sek D. (ref22/cit22) 2013; 117 Wang F. F. (ref10/cit10) 2012; 48 Liu L. (ref11/cit11) 2008; 10 Mahtab F. (ref12/cit12) 2011; 10 Baldo M. A. (ref7/cit7) 2000; 403 |
References_xml | – volume: 129 start-page: 2669 year: 2007 ident: ref6/cit6 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja0680257 contributor: fullname: Kim S. – start-page: 1740 year: 2001 ident: ref9/cit9 publication-title: Chem. Commun. doi: 10.1039/b105159h contributor: fullname: Luo J. D. – volume: 135 start-page: 4926 year: 2013 ident: ref13/cit13 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja400337p contributor: fullname: Chen S. J. – volume: 21 start-page: 13470 year: 2011 ident: ref19/cit19 publication-title: J. Mater. Chem. doi: 10.1039/c1jm12098k contributor: fullname: Song P. S. – volume: 108 start-page: 10887 year: 2004 ident: ref23/cit23 publication-title: J. Phys. Chem. B doi: 10.1021/jp0488012 contributor: fullname: Li S. Y. – volume: 28 start-page: 1439 year: 2012 ident: ref26/cit26 publication-title: Langmuir doi: 10.1021/la202755z contributor: fullname: Javed I. – volume: 10 start-page: 4581 year: 2008 ident: ref11/cit11 publication-title: Org. Lett. doi: 10.1021/ol801855s contributor: fullname: Liu L. – volume: 105 start-page: 1491 year: 2005 ident: ref1/cit1 publication-title: Chem. Rev. doi: 10.1021/cr030070z contributor: fullname: Hoeben F. J. M. – volume: 107 start-page: 1339 year: 2007 ident: ref8/cit8 publication-title: Chem. Rev. doi: 10.1021/cr0501339 contributor: fullname: Thomas S. W. – volume: 1 start-page: 1310 year: 2013 ident: ref20/cit20 publication-title: J. Mater. Chem. A doi: 10.1039/C2TA00574C contributor: fullname: Shellaiah M. – volume: 403 start-page: 750 year: 2000 ident: ref7/cit7 publication-title: Nature doi: 10.1038/35001541 contributor: fullname: Baldo M. A. – volume: 127 start-page: 4548 year: 2005 ident: ref3/cit3 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja050168q contributor: fullname: Li C. – volume: 295 start-page: 2418 year: 2002 ident: ref2/cit2 publication-title: Science doi: 10.1126/science.1070821 contributor: fullname: Whitesides G. M. – volume: 10 start-page: 1448 year: 2011 ident: ref12/cit12 publication-title: Small doi: 10.1002/smll.201002195 contributor: fullname: Mahtab F. – volume: 117 start-page: 10320 year: 2013 ident: ref22/cit22 publication-title: J. Phys. Chem. A doi: 10.1021/jp407623u contributor: fullname: Sek D. – volume: 74 start-page: 2163 year: 2009 ident: ref18/cit18 publication-title: J. Org. Chem. doi: 10.1021/jo802631m contributor: fullname: Tang W. X. – volume: 48 start-page: 7395 year: 2012 ident: ref10/cit10 publication-title: Chem. Commun. doi: 10.1039/c2cc33172a contributor: fullname: Wang F. F. – volume: 85 start-page: 1465 year: 2013 ident: ref21/cit21 publication-title: Pure Appl. Chem. doi: 10.1351/PAC-CON-13-02-06 contributor: fullname: Yang G. Q. – volume: 33 start-page: 4610 year: 2000 ident: ref5/cit5 publication-title: Macromolecules doi: 10.1021/ma000100p contributor: fullname: Chen X. L. – volume: 102 start-page: 1902 year: 1998 ident: ref28/cit28 publication-title: J. Phys. Chem. B doi: 10.1021/jp973225d contributor: fullname: Oelkrug D. – volume: 131 start-page: 3950 year: 2009 ident: ref25/cit25 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja806162h contributor: fullname: An B. K. – volume: 27 start-page: 2844 year: 2011 ident: ref27/cit27 publication-title: Langmuir doi: 10.1021/la104302d contributor: fullname: Chahine J. – volume: 13 start-page: 14960 year: 2011 ident: ref24/cit24 publication-title: Phys. Chem. Chem. Phys. doi: 10.1039/c1cp21039d contributor: fullname: Randino C. – volume: 132 start-page: 9268 year: 2010 ident: ref4/cit4 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja1027502 contributor: fullname: Yan Q. – volume: 23 start-page: 5430 year: 2011 ident: ref14/cit14 publication-title: Adv. Mater. doi: 10.1002/adma.201102804 contributor: fullname: Zhao Z. J. – volume: 26 start-page: 6838 year: 2010 ident: ref15/cit15 publication-title: Langmuir doi: 10.1021/la904727t contributor: fullname: Lu H. G. – volume: 23 start-page: 3261 year: 2011 ident: ref16/cit16 publication-title: Adv. Mater. doi: 10.1002/adma.201101059 contributor: fullname: Luo X. L. – volume: 22 start-page: 3406 year: 2012 ident: ref17/cit17 publication-title: Small contributor: fullname: Gu X. G. |
SSID | ssj0009349 |
Score | 2.4157503 |
Snippet | Four electron-donor-substituted aggregation-induced emission (AIE) compounds, N,N′-bis(4-methoxylsalicylidene)-p-phenylenediamine (BSPD-OMe),... Four electron-donor-substituted aggregation-induced emission (AIE) compounds, N,N'-bis(4-methoxylsalicylidene)-p-phenylenediamine (BSPD-OMe),... |
SourceID | proquest crossref pubmed acs |
SourceType | Aggregation Database Index Database Publisher |
StartPage | 2351 |
Title | Color- and Morphology-Controlled Self-Assembly of New Electron-Donor-Substituted Aggregation-Induced Emission Compounds |
URI | http://dx.doi.org/10.1021/la404436v https://www.ncbi.nlm.nih.gov/pubmed/24571508 https://search.proquest.com/docview/1506791473 |
Volume | 30 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwhV3HTsQwEB1RDnChl6XJlKshcUk5orAIIcEFkLhFdmxzYEnQFhB8PeNkQxHtFiWxY3vsmWfP5A3AgUaMbBCYU2YTS4XDK8UTSbkLuHBGClGn6by4jM5uxPmtvJ2A_V88-Cw86ikRCMGjp0mYZjEuCo9_sqsPZl3eYFzPtRmLiLf0QZ-LetNTDL6anl_wZG1XTufhpP07pwknuT8cDfVh8fqdrPGvJi_A3BhXkuNmIizChC2XYCZr07ktw3OGaq5PiSoNuahwdOvzdJo1oeo9a8iV7TnqncAPuvdCKkdQAZLuOE0OPalKLO71TBNcYMjxHe7V72rJUp8BpMB7XfycP38jXs_4jE2DFbg57V5nZ3ScdcELKRxSY9Io5qnVCpEA0zpJI8ki66LUKs0kCwoTFLEVQZEyg4DJxEJrg6ZWWmfRuvFVmCqr0q4DSYxTJi0QpeGmTEZpIlNlnFOhCY3AJx3YQbHk41UzyGuHOAvz9_HrwF4rsfyxYd_46aXdVpY5dtI7PFRpqxHWJ_0xWShi3oG1Rsjv1TAhY8-Fv_FfGzZhFkGS8HFnYbgFU8P-yG4jEBnqnXoivgFH5diV |
link.rule.ids | 315,783,787,2772,27088,27936,27937,57066,57116 |
linkProvider | American Chemical Society |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1LT4QwEG58HPTi-7E-q_FaBdryOBpcs-quFzXxRlraenAFI7sa_fVOC7s-otEbAVqGTpn52hm-QehAAkZWAMxJoGNNmIEjQWNOqPEoM4oz5sp09i7Dzg07v-W3DU2O_RcGhKigp8oF8T_YBfyjvmAeYzR8nkTTPAJHaWFQevVBsEtrqGspNyMW0hGL0Oem1gPl1VcP9AusdO7ldL6uU-QEc1kl94fDgTzM375xNv5P8gU016BMfFxPi0U0oYslNJOOirsto5cUjN4TwaJQuFfCWLvddZLWiet9rfCV7htiQ8IPsv-KS4PBHOJ2UzSHnJQFNLdWp041UPj4Dlbud07PxNYDyeFcGx5nd-OwtTq2flO1gm5O29dphzQ1GKzK_AFRKgkjmmgpABcEUsZJyINQmzDRQgY88HLl5ZFmXp4ECuCTipiUChwv10aDr6OraKooC72OcKyMUEkOmA2WaDxMYp4IZYzwla8YXGmhHRi-rPmGqsyFxwM_G49fC-2PFJc91lwcP920N1JpBi9pwx-i0OUQ-uN208xnEW2htVrX424CxiPLjL_xlwy7aKZz3etm3bPLi000C_CJ2Yw0399CU4Onod4GiDKQO25uvgPnvOD6 |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1Lb9QwEB5BkaAX3tDlUQzi6jaO7TyOq3RX5dGCVCr1FtkZuweWpGp2QfDrGTvZ5SEQ3KIkdsYee-Ybz2QG4KUljIwEzHnqCseVpysjC82lT6TyqJWKZTqPjrPDU_X6TJ-NhmL4F4aI6KmnPjrxw66-QD9mGBD7C6MSpWT2-Spc07mIbtlpdfIjya4c4G5Iu5mrTK4zCf3cNGihpv9VC_0FWkYVM78F7zbExciSj3urpd1rvv2Wt_H_qb8NN0e0yabD8rgDV1x7F25U6yJv9-BLRcLvkjPTIjvqaM7jKTuvhgD2hUN24haeB9fwJ7v4yjrPSCyy2Vg8hx90LTUP0mcIOUA2PScL_jzym4e6IA3dm9HnwqkcC9In1HHq78PpfPahOuRjLYbAOrHkiGWWy9JZQ_ggtbYoM51mzmelMzbVadJg0uROJU2ZIsEozJW1SApYO-9I58kHsNV2rdsBVqA3WDaE3chU01lZ6NKg90agQEVPJrBLU1iPe6mvo5s8FfVm_ibwYs28-mLIyfGnl56v2VrTIIMbxLSuW1F_OhyeCZXLCTwc-L3pJlW0rgizPvoXDc_g-vuDef321fGbx7BNKEqFwDQhnsDW8nLlnhJSWdrduDy_Ayt343Q |
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=Color-+and+Morphology-Controlled+Self-Assembly+of+New+Electron-Donor-Substituted+Aggregation-Induced+Emission+Compounds&rft.jtitle=Langmuir&rft.au=Niu%2C+Caixia&rft.au=Zhao%2C+Liu&rft.au=Fang%2C+Tao&rft.au=Deng%2C+Xuebin&rft.date=2014-03-11&rft.issn=0743-7463&rft.eissn=1520-5827&rft.volume=30&rft.issue=9&rft.spage=2351&rft.epage=2359&rft_id=info:doi/10.1021%2Fla404436v&rft.externalDBID=n%2Fa&rft.externalDocID=10_1021_la404436v |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0743-7463&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0743-7463&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0743-7463&client=summon |