ESR CHARACTERIZATION OF OLIGOMERIC THIOPHENE MATERIALS

被引:16
作者
DIERS, JR
DEARMOND, MK
GUAY, J
DIAZ, A
WU, RL
SCHUMM, JS
TOUR, JM
机构
[1] NEW MEXICO STATE UNIV,DEPT CHEM & BIOCHEM,LAS CRUCES,NM 88003
[2] IBM CORP,ALMADEN RES CTR,SAN JOSE,CA 95102
[3] UNIV S CAROLINA,DEPT CHEM & BIOCHEM,COLUMBIA,SC 29208
关键词
D O I
10.1021/cm00039a013
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The ESR of electrooxidation products of orthogonally bridged dimers of alpha,alpha-coupled thiophene oligomers and spiro-fused phenylene-thiophene mixed oligomers was studied as a function of temperature. ESR measurements on the one-electron oxidation products indicate that the charge remains on a single oligomer unit and does not hop between the two bridged oligomer chains for temperatures up to 300 K. This is evident from the presence of hyperfine structure in ESR spectra for the dimers of short-chain oligomers and the small temperature-dependent line broadening for longer chain spiro dimers, characteristic of a low-energy process such as the paramagnetic site moving along the oligomer chain length. The activation energy for a paramagnetic center moving along the oligomer chain length has been estimated at <100 cm-1. The incorporation of phenylene into the oligomer unit shifts oxidation potentials anodic and also inhibits the mobility of the polaron along the pihconjugated oligomer segment. Evidence for formation of pi-pi dimers in solutions of 7-mT has also been obtained.
引用
收藏
页码:327 / 332
页数:6
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