Linear organic π-conjugated systems featuring the heavy Group 14 and 15 elements

被引:324
作者
Hissler, M
Dyer, PW
Réau, R
机构
[1] Univ Leicester, Dept Chem, Leicester LE1 7RH, Leics, England
[2] Univ Rennes 1, Inst Chim, CNRS, UMR 6509, F-35042 Rennes, France
关键词
pi-conjugated polymers; heteroelements; electronic structure; metalloles;
D O I
10.1016/S0010-8545(03)00098-5
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
An overview of the synthesis and properties of linear organic pi-conjugated systems featuring Group 14 and 15 moieties is presented and comparisons made with their better-known hydrocarbon, and nitrogen- and sulfur-containing analogues. The major focus of this review is pi-conjugated systems based on heteroles. The unique electronic structure and nature of siloles and phospholes is examined, highlighting the influence of both the ring substituents and the character of the heteroatom on their photophysical properties. The synthesis of a variety of Group 14 and 15 heterole building blocks suitable for the construction of pi-conjugated systems is presented. The preparation and physical properties of poly- and oligo-(1,1-silole)s and -(2,5-silole)s, oligo-(2,5-phosphole)s and co-oligomers of silole and phosphole blocks with other electron-rich monomer units, all with extended pi-conjugation, are discussed. A brief resume of linear pi-conjugated materials that possess heavy Group 15 elements in the polymer backbone is also presented. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 44
页数:44
相关论文
共 237 条
[1]   Organic electroluminescence of silole-incorporated polysilane [J].
Adachi, A ;
Yasuda, H ;
Sanji, T ;
Sakurai, H ;
Okita, K .
JOURNAL OF LUMINESCENCE, 2000, 87-9 (87) :1174-1176
[2]   Large molecular hyperpolarizabilities. Quantitative analysis of aromaticity and auxiliary donor-acceptor effects [J].
Albert, IDL ;
Marks, TJ ;
Ratner, MA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (28) :6575-6582
[3]  
[Anonymous], 1986, Handbook of Conducting Polymers
[4]  
[Anonymous], COMPREHENSIVE HETERO
[5]  
[Anonymous], 1986, Handbook of Conducting Polymers
[6]  
Apperloo JJ, 2000, CHEM-EUR J, V6, P1698, DOI 10.1002/(SICI)1521-3765(20000502)6:9<1698::AID-CHEM1698>3.3.CO
[7]  
2-I
[8]  
ARMITAGE DA, 1996, COMPREHENSIVE HETERO, P903
[9]   SYNTHESIS AND CRYSTAL AND MOLECULAR-STRUCTURE OF 2,5-BIS(TRIMETHYLSILYL)-3,4-DIMETHYL-1-BISMAFERROCENE - AN AROMATIC HETEROCYCLE CONTAINING BISMUTH [J].
ASHE, AJ ;
KAMPF, JW ;
ALTAWEEL, SM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (01) :372-374
[10]   Electrochemistry and polymerization mechanisms of thiophene-pyrrole-thiophene oligomers and terthiophenes. Experimental and theoretical modeling studies [J].
Audebert, P ;
Catel, JM ;
Le Coustumer, G ;
Duchenet, V ;
Hapiot, P .
JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (44) :8661-8669