Hole-Transfer Dyads and Triads Based on Perylene Monoimide, Quaterthiophene, and Extended Tetrathiafulvalene

被引:18
作者
Boixel, Julien [1 ]
Blart, Errol [1 ]
Pellegrin, Yann [1 ]
Odobel, Fabrice [1 ]
Perin, Nicola [2 ]
Chiorboli, Claudio [3 ]
Fracasso, Sandro [2 ]
Ravaglia, Marcella [2 ]
Scandola, Franco [2 ,4 ]
机构
[1] Univ Nantes, CNRS, UMR 6230, F-44322 Nantes 3, France
[2] Univ Ferrara, Dipartimento Chirurg, I-44100 Ferrara, Italy
[3] ISOF CNR, Sez Ferrara, I-44100 Ferrara, Italy
[4] Ctr Ric Interuniv Convers Chim Energia Solare, Sez Ferrara, I-44100 Ferrara, Italy
关键词
charge separation; donor-acceptor systems; electron transfer photophysics; time-resolved spectroscopy; PHOTOINDUCED ELECTRON-TRANSFER; MOLECULAR-ORBITAL METHODS; OLIGOTHIOPHENE-FULLERENE TRIADS; PHOTOSYNTHETIC REACTION-CENTER; CHARGE-TRANSFER PROCESSES; GAUSSIAN-TYPE BASIS; ARTIFICIAL PHOTOSYNTHESIS; PHOTOVOLTAIC APPLICATIONS; ENERGY-CONVERSION; ORGANIC-MOLECULES;
D O I
10.1002/chem.201000640
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two families of dyad and triad systems based on perylene monoimide (PM I), quaterthiophene (QT), and 9,10-bis(1,3-dithiol-2-ylidene)-9,10-dihydroanthracene (extended tetrathiafulvalene, exTTF) molecular components have been designed and synthesized. The dyads (D1 and D2) are of the PMI-QT type and the triads (T1 and T2) of the PMI-QT-exTTF type. The two families differ in the saturated or unsaturated nature of the linker groups (ethynylene in D1 and T1, ethylene in D2 and T2) that bridge the molecular components. The dyads and triads have been characterized by electrochemical, photophysical, and computational methods. Both the experimental and the computational (DFT) results indicate that in the unsaturated systems strong intercomponent interactions lead to substantial perturbation of the properties of the subunits. In particular, in T1, delocalization is particularly effective between the QT and exTTF units, which would be better viewed combined as a single electronic subsystem. For the dyad systems, the photophysics observed following excitation of the PMI unit is solvent-dependent. In moderately polar solvents (dichloromethane, diethyl ether) fast charge separation is followed by recombination to the ground state. In toluene, slow conversion to the charge-separated state is followed by intersystem crossing and recombination to yield the triplet state of the PMI unit. The behavior of the triads, on the other hand, is remarkably similar to that of the corresponding dyads, which indicates that, after primary charge separation, hole shift from the oxidized QT component to exTTF is quite inefficient. This unexpected result has been rationalized on the basis of the anomalous (simultaneous two-electron oxidation) electrochemistry of exTTF and with the help of DFT calculations. In fact, although exTTF is electrochemically easier to oxidize than QT by around 0.6 V. the one-electron redox orbitals (HOMOs) of the two units in triad T2 are almost degenerate.
引用
收藏
页码:9140 / 9153
页数:14
相关论文
共 81 条
[1]   Design of near-infrared dyes based on π-conjugation system extension 2.: Theoretical elucidation of framework extended derivatives of perylene chromophore [J].
Adachi, M ;
Nagao, Y .
CHEMISTRY OF MATERIALS, 2001, 13 (02) :662-669
[2]   Tuning electron transfer through p-phenyleneethynylene molecular wires [J].
Atienza, Carmen ;
Martin, Nazario ;
Wielopolski, Mateusz ;
Haworth, Naomi ;
Clark, Timothy ;
Guldi, Dirk M. .
CHEMICAL COMMUNICATIONS, 2006, (30) :3202-3204
[3]   Determination of the attenuation factor in fluorene-based molecular wires [J].
Atienza-Castellanos, Carmen ;
Wielopolski, Mateusz ;
Guldi, Dirk M. ;
van der Pol, Cornelia ;
Bryce, Martin R. ;
Filippone, Salvatore ;
Martin, Nazario .
CHEMICAL COMMUNICATIONS, 2007, (48) :5164-5166
[4]  
Balzani V., 2001, ELECT TRANSFER CHEM, V1
[5]  
Balzani V.S. F., 1991, Supramolecular Photochemistry
[6]   Photochemical conversion of solar energy [J].
Balzani, Vincenzo ;
Credi, Alberto ;
Venturi, Margherita .
CHEMSUSCHEM, 2008, 1 (1-2) :26-58
[7]   From ruthenium(II) to iridium(III): 15 years of triads based on bis-terpyridine complexes [J].
Baranoff, E ;
Collin, JP ;
Flamigni, L ;
Sauvage, JP .
CHEMICAL SOCIETY REVIEWS, 2004, 33 (03) :147-155
[8]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[9]   Active transport of Ca2+ by an artificial photosynthetic membrane [J].
Bennett, IM ;
Farfano, HMV ;
Bogani, F ;
Primak, A ;
Liddell, PA ;
Otero, L ;
Sereno, L ;
Silber, JJ ;
Moore, AL ;
Moore, TA ;
Gust, D .
NATURE, 2002, 420 (6914) :398-401
[10]   Fast evaluation of geometries and properties of excited molecules in solution: A Tamm-Dancoff model with application to 4-dimethylaminobenzonitrile [J].
Cammi, R ;
Mennucci, B ;
Tomasi, J .
JOURNAL OF PHYSICAL CHEMISTRY A, 2000, 104 (23) :5631-5637