Hexadecadehydrodibenzo[20]-, Tetracosadehydrotribenzo[30]-, and Dotriacontadehydrotetrabenzo[40]annulenes: Syntheses, Characterizations, Electronic Properties, and Self-Associations

被引:15
作者
Kato, Shin-ichiro [1 ]
Takahashi, Nobutaka [1 ]
Nakamura, Yosuke [1 ]
机构
[1] Gunma Univ, Div Mol Sci, Fac Sci & Technol, Kiryu, Gunma 3768515, Japan
关键词
DEHYDROBENZOANNULENES; GENERATION; BEHAVIOR; MODEL;
D O I
10.1021/jo401200m
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Hexadecadehydrodibenzo[20]-, tetracosadehydrotribenzo[30]-, and dotriacontadehydrotetrabenzo[40]annulene derivatives ([20]-, [30]-, and [40]DBAs) possessing tetrayne linkages were synthesized. X-ray diffraction analysis demonstrated that the molecules of [30]DBA and p-xylene form a 2D sheetlike structure. Planar [20]- and [30]DBAs show significantly weak or almost no tropicity. The extension of the acetylenic linkages from a diyne to a tetrayne unit narrows HOMO-LUMO gaps. The self-association behavior of [30]DBA in solution resulting from effective pi-pi stacking interactions was observed.
引用
收藏
页码:7658 / 7663
页数:6
相关论文
共 40 条
[1]   A versatile synthetic route to dehydrobenzoannulenes via in situ generation of reactive alkynes [J].
Bell, ML ;
Chiechi, RC ;
Johnson, CA ;
Kimball, DB ;
Matzger, AJ ;
Wan, WB ;
Weakley, TJR ;
Haley, MM .
TETRAHEDRON, 2001, 57 (17) :3507-3520
[2]  
Bunz UHF, 1999, CHEM-EUR J, V5, P263, DOI 10.1002/(SICI)1521-3765(19990104)5:1<263::AID-CHEM263>3.0.CO
[3]  
2-X
[4]  
Chalifoux WA, 2010, NAT CHEM, V2, P967, DOI [10.1038/NCHEM.828, 10.1038/nchem.828]
[5]   Fluorescent supramolecular polymers:: Metal directed self-assembly of perylene bisimide building blocks [J].
Dobrawa, R ;
Lysetska, M ;
Ballester, P ;
Grüne, M ;
Würthner, F .
MACROMOLECULES, 2005, 38 (04) :1315-1325
[6]  
EGLINTON G, 1957, P CHEM SOC LONDON, P350
[7]  
Frisch M, 2015, Gaussian 09, revision a 02
[8]   Synthesis of linearly-fused benzodehydro[12]annulenes [J].
Gallagher, ME ;
Anthony, JE .
TETRAHEDRON LETTERS, 2001, 42 (43) :7533-7536
[9]  
Gibtner T, 2002, CHEM-EUR J, V8, P408, DOI 10.1002/1521-3765(20020118)8:2<408::AID-CHEM408>3.3.CO
[10]  
2-C