Fluorescent Dendritic Organogels Based on 2-(2′-Hydroxyphenyl)benzoxazole: Emission Enhancement and Multiple Stimuli-Responsive Properties

被引:63
作者
Chen, Hui [1 ,2 ,3 ]
Feng, Yu [2 ]
Deng, Guo-Jun [1 ,3 ]
Liu, Zhi-Xiong [2 ,3 ]
He, Yan-Mei [2 ,3 ]
Fan, Qing-Hua [2 ,3 ]
机构
[1] Xiangtan Univ, Key Lab Environm Friendly Chem & Applicat, Minist Educ, Coll Chem, Xiangtan 411105, Peoples R China
[2] Chinese Acad Sci, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
[3] Chinese Acad Sci, CAS Key Lab Mol Recognit & Funct, Inst Chem, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
aggregation; dendrimers; fluorescence; multiresponsiveness; sol-gel processes; supramolecular chemistry; INTRAMOLECULAR PROTON-TRANSFER; POLY(BENZYL ETHER) DENDRONS; SUPRAMOLECULAR GELS; TRANSFER ESIPT; HIGHLY EFFICIENT; GELATION; MULTISTIMULI; GELATORS; TRANSITION; DESIGN;
D O I
10.1002/chem.201500849
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new highly efficient and versatile poly(benzyl ether) dendritic organogelator HPB-G(1) with 2-(2'-hydroxyphenyl) benzoxazole (HPB) at the focal point has been designed and synthesized. HPB-G(1) can form stable organogels toward various apolar and polar organic solvents. Further studies revealed that intermolecular multiple pi-pi stacking interactions are the main driving forces for the formation of the organogels. Notably, dendron HPB-G(1) exhibited a significantly enhanced emission in the gel state in contrast to weak emission in solution. Most interestingly, these dendritic organogels exhibited multiple stimuli-responsive behaviors upon exposure to environmental stimuli, including temperature, sonication, shear stress, and the presence of anions, metal cations, acids/ bases, thus leading to reversible sol-gel phase transitions.
引用
收藏
页码:11018 / 11028
页数:11
相关论文
共 110 条
[1]  
[Anonymous], 2001, ANGEW CHEM
[2]  
[Anonymous], ANGEW CHEM
[3]  
Babu S. S., 2012, ANGEW CHEM, V124, P1800
[4]   Excited State Processes in Linear π-System-Based Organogels [J].
Babu, Sukumaran S. ;
Kartha, Kalathil K. ;
Ajayaghosh, Ayyappanpillai .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2010, 1 (23) :3413-3424
[5]   Functional π-Gelators and Their Applications [J].
Babu, Sukumaran Santhosh ;
Praveen, Vakayil K. ;
Ajayaghosh, Ayyappanpillai .
CHEMICAL REVIEWS, 2014, 114 (04) :1973-2129
[6]   Effect of the Bulkiness of the End Functional Amide Groups on the Optical, Gelation, and Morphological Properties of Oligo(p-phenylenevinylene) π-Gelators [J].
Babu, Sukumaran Santhosh ;
Praveen, Vakayil K. ;
Kartha, Kalathil K. ;
Mahesh, Sankarapillai ;
Ajayaghosh, Ayyappanpillai .
CHEMISTRY-AN ASIAN JOURNAL, 2014, 9 (07) :1830-1840
[7]   Self-Assembled Gelators for Organic Electronics [J].
Babu, Sukumaran Santhosh ;
Prasanthkumar, Seelam ;
Ajayaghosh, Ayyappanpillai .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2012, 51 (08) :1766-1776
[8]   Supramolecular gels 'in action' [J].
Banerjee, Supratim ;
Das, Rajat K. ;
Maitra, Uday .
JOURNAL OF MATERIALS CHEMISTRY, 2009, 19 (37) :6649-6687
[9]   Ultrasound induced gelation: a paradigm shift [J].
Bardelang, David .
SOFT MATTER, 2009, 5 (10) :1969-1971
[10]   Multistimuli, multiresponsive metallo-supramolecular polymers [J].
Beck, JB ;
Rowan, SJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (46) :13922-13923