4-substituted push-pull quinazoline chromophores with extended π-conjugated linker

被引:4
|
作者
Bonnaud, Thibault [1 ]
Scaviner, Mathieu [1 ]
Robin-le Guen, Francoise [1 ]
Achelle, Sylvain [1 ,2 ]
机构
[1] Univ Rennes, IRISA, CNRS, Rennes, France
[2] Univ Rennes, ISCR Inst Sci Chim Rennes UMR 6226, Sylvain Achelle, CNRS, F-35000 Rennes, France
关键词
DERIVATIVES; PHOTOLUMINESCENCE; COMPLEXES; DESIGN; DYES;
D O I
10.1002/jhet.4768
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A series of four push-pull compounds based on a 4-phenylquinazoline scaffold were designed. Three of these compounds exhibit dual state emission with intense fluorescence in solution and solid state. Their emission properties are sensible to environement stimuli with intense emission solvatochromism and halochromism. In case of methoxy derivative, both neutral and protonated form are luminescent and white light emission can be observed by controlled partial protonation. 4-substituted quinazoline push-pull derivatives were designed and exhibit emisison solvatochromism, halochromism and solid state emission.image
引用
收藏
页码:358 / 364
页数:7
相关论文
共 50 条
  • [41] Incorporation of zwitterionic push-pull chromophores into hybrid organic - Inorganic matrixes
    Innocenzi, P
    Miorin, E
    Brusatin, G
    Abbotto, A
    Beverina, L
    Pagani, GA
    Casalboni, M
    Sarcinelli, F
    Pizzoferrato, R
    CHEMISTRY OF MATERIALS, 2002, 14 (09) : 3758 - 3766
  • [42] N, N′-Dibutylbarbituric acid as an acceptor moiety in push-pull chromophores
    Klikar, Milan
    Bures, Filip
    Pytela, Oldrich
    Mikysek, Tomas
    Padelkova, Zdenka
    Barsella, Alberto
    Dorkenoo, Kokou
    Achelle, Sylvain
    NEW JOURNAL OF CHEMISTRY, 2013, 37 (12) : 4230 - 4240
  • [43] Understanding non-linearity: a simple model for push-pull chromophores
    Painelli, A
    Del Freo, L
    Terenziani, F
    SYNTHETIC METALS, 2001, 121 (1-3) : 1465 - 1466
  • [45] Imidazole as a central π-linkage in Y-shaped push-pull chromophores
    Kulhanek, Jiri
    Bures, Filip
    Mikysek, Tomas
    Ludvik, Jiri
    Pytela, Oldrich
    DYES AND PIGMENTS, 2011, 90 (01) : 48 - 55
  • [46] Influence of electronic acceptor on the excited state properties of push-pull chromophores
    Chi, Xiao-Chun
    Ni, Mou-Cui
    Wang, Ying-Hui
    Sui, Ning
    Wang, Wen-Yan
    Lu, Ran
    Yang, Yan-Qiang
    Ji, Wen-Yu
    Zhang, Han-Zhuang
    JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2017, 346 : 221 - 224
  • [47] BODIPY-Bridged Push-Pull Chromophores for Nonlinear Optical Applications
    Ulrich, Gilles
    Barsella, Alberto
    Boeglin, Alex
    Niu, Songlin
    Ziessel, Raymond
    CHEMPHYSCHEM, 2014, 15 (13) : 2693 - 2700
  • [48] Alphabet-Inspired Design of (Hetero)Aromatic Push-Pull Chromophores
    Klikar, Milan
    Solanke, Parmeshwar
    Tydlitat, Jiri
    Bures, Filip
    CHEMICAL RECORD, 2016, 16 (04): : 1886 - 1905
  • [49] A non-pertubative approach to solvatochromic shifts of push-pull chromophores
    Painelli, A
    Terenziani, F
    CHEMICAL PHYSICS LETTERS, 1999, 312 (2-4) : 211 - 220
  • [50] New non-planar push-pull chromophores: Synthesis and characterization
    Chiu, Melanie
    Kivala, Milan
    Kato, Shin-ichiro
    Diederich, Francois
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2010, 240