Open-Shell Ground State of Polyacenes: A Valence Bond Study

被引:84
作者
Qu, Zexing [1 ]
Zhang, Dawei [1 ]
Liu, Chungen [1 ]
Jiang, Yuansheng [1 ]
机构
[1] Nanjing Univ, Inst Theoret & Computat Chem, Key Lab Mesoscop Chem, MOE,Sch Chem & Chem Engn, Nanjing 210093, Peoples R China
关键词
QUANTUM RENORMALIZATION-GROUPS; EVAPORATED PENTACENE FILMS; ELECTRONIC-STRUCTURES; LINEAR POLYACENES; CARBON SKELETONS; HIGHER ACENES; AB-INITIO; POLYMERS; SINGLET; HYDROCARBONS;
D O I
10.1021/jp9015728
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
Applying the density matrix renormalization group (DRMG) method to a nonempirical valence bond (VB) model Hamiltonian, we studied polyacene oligomers of different lengths in the strong electron correlation limit. Geometrical optimizations were performed for the lowest singlet and triplet states of oligomers up to [40]-acene, and a convergence of the bond lengths toward the polymer limit is observed in the interior of the oligomer. For large oligomers, as well as for the polymer, the ground state can be reasonably determined to be a singlet. Furthermore, a high similarity between the singlet geometries and triplet geometries suggests ail open-shell character for the singlet ground state. A reasonable speculation of the soliton-antisoliton pair character of the singlet ground state was supported by a spin distribution analysis of the triplet state wave function of large oligomers, with each of the two solitons being broadly delocalized over the upper or bottom edge of the oligomers, respectively.
引用
收藏
页码:7909 / 7914
页数:6
相关论文
共 55 条
[1]   ELECTRONIC-STRUCTURE OF LINEAR POLYACENES IN SCF RPA METHOD [J].
BALDO, M ;
GRASSI, A ;
PUCCI, R ;
TOMASELLO, P .
JOURNAL OF CHEMICAL PHYSICS, 1982, 77 (05) :2438-2444
[2]  
BALDO M, 1983, PHYS LETT A, V95, P261
[3]   Attempts to model neutral solitons in polyacetylene by ab initio and density functional methods.: The nature of the spin distribution in polyenyl radicals [J].
Bally, T ;
Hrovat, DA ;
Borden, WT .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2000, 2 (15) :3363-3371
[4]   Tetrathiafulvalenes, oligoacenenes, and their buckminsterfullerene derivatives: The brick and mortar of organic electronics [J].
Bendikov, M ;
Wudl, F ;
Perepichka, DF .
CHEMICAL REVIEWS, 2004, 104 (11) :4891-4945
[5]   Oligoacenes: Theoretical prediction of open-shell singlet diradical ground states [J].
Bendikov, M ;
Duong, HM ;
Starkey, K ;
Houk, KN ;
Carter, EA ;
Wudl, F .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (24) :7416-7417
[6]   DIELS-ALDER REACTIVITY OF POLYCYCLIC AROMATIC-HYDROCARBONS .1. ACENES AND BENZOLOGS [J].
BIERMANN, D ;
SCHMIDT, W .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (09) :3163-3173
[7]   BOND LENGTH ALTERNATION IN INFINITELY LONG CONJUGATED POLYACENES [J].
BOON, MR .
THEORETICA CHIMICA ACTA, 1971, 23 (01) :109-&
[8]  
BOOVIC I, 1985, PHYS REV B, V32, P8136
[9]   EFFECTS OF ELECTRON REPULSION IN CONJUGATED HYDROCARBON DIRADICALS [J].
BORDEN, WT ;
DAVIDSON, ER .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1977, 99 (14) :4587-4594
[10]  
BURGOS J, 1977, STATUS SOLIDI B, V83, P294