Tetrathiafulvalene-Polychlorotriphenylmethyl Dyads: Influence of Bridge and Open-Shell Characteristics on Linear and Nonlinear Optical Properties

被引:19
|
作者
Souto, Manuel [1 ]
Calbo, Joaquin [2 ]
Ratera, Imma [1 ]
Orti, Enrique [2 ]
Veciana, Jaume [1 ]
机构
[1] UAB, CSIC, ICMAB, Inst Ciencia Mat Barcelona,CIBER, BBN Campus Univ, Bellaterra 08193, Spain
[2] Univ Valencia, Inst Ciencia Mol, Paterna 46980, Spain
关键词
donor-acceptor complexes; intramolecular charge transfer; nonlinear optics; PTM radicals; tetrathiafulvalene; FUNCTIONAL RESPONSE THEORY; EXCITATION-ENERGIES; DERIVATIVES; STATES; REDOX; DONOR; DESIGN; COMPLEXES; RADICALS; SPIN;
D O I
10.1002/chem.201701623
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Three conjugated donor--acceptor radical systems (1a-1c) were prepared by bridging a tetrathiafulvalene (TTF) electron-donor unit to a polychlorotriphenylmethyl (PTM) electron-acceptor radical through vinylene units of different lengths. The dependence of the intramolecular charge transfer on the length of the conjugated bridge has been analyzed by different electrochemical and spectroscopic techniques. Linear optical properties and the second-order nonlinear optical (NLO) response of these derivatives have been computed by comparing systems 1a-1c with the non-radical analogues (2a-2c). Interestingly, an enhanced NLO response is predicted for dyads 1a-1c with PTM in the radical form and for compounds with longer vinylene bridges. Calculations confirm the active role the bridge plays for electronic communication between the donor TTF and the acceptor PTM units.
引用
收藏
页码:11067 / 11075
页数:9
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