A quadruply azulene-fused porphyrin with intense near-IR absorption and a large two-photon absorption cross section

被引:251
作者
Kurotobi, Kei
Kim, Kil Suk
Noh, Su Bum
Kim, Dongho [1 ]
Osuka, Atsuhiro
机构
[1] Yonsei Univ, Dept Chem, Ctr Ultrafast Opt Characterist Control, Seoul 120749, South Korea
[2] Kyoto Univ, Dept Chem, Grad Sch Sci, Kyoto, Japan
[3] CREST, Japan Sci & Technol Agcy, Sakyo Ku, Kyoto 6068502, Japan
关键词
azulenes; fused-ring systems; optical properties; porphyrinoids; two-photon absorption;
D O I
10.1002/anie.200600892
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
(Chemical Equation Presented) Extending conjugation: Azulene-fused porphyrins (see example) are synthesized through the oxidation of meso-(4-azulenyl)porphyrins with FeCl3. The azulene-fused strategy allowed highly π-conjugated porphyrinic electronic systems, which are promising two-photon absorption pigments, to be realized. © 2006 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:3944 / 3947
页数:4
相关论文
共 62 条
[1]   Relationship between two-photon absorption and the π-conjugation pathway in porphyrin arrays through dihedral angle control [J].
Ahn, TK ;
Kim, KS ;
Kim, DY ;
Noh, SB ;
Aratani, N ;
Ikeda, C ;
Osuka, A ;
Kim, D .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (05) :1700-1704
[2]  
Aihara H, 2001, ANGEW CHEM INT EDIT, V40, P3439, DOI 10.1002/1521-3773(20010917)40:18<3439::AID-ANIE3439>3.0.CO
[3]  
2-Z
[4]  
AIHARA H, 2001, ANGEW CHEM, V113, P3547
[5]   Building molecular wires from the colours of life: conjugated porphyrin oligomers [J].
Anderson, HL .
CHEMICAL COMMUNICATIONS, 1999, (23) :2323-2330
[6]  
[Anonymous], [No title captured], DOI DOI 10.1107/S0108767389011189
[7]  
[Anonymous], ANGEW CHEM
[8]  
Aratani N, 2000, ANGEW CHEM INT EDIT, V39, P1458, DOI 10.1002/(SICI)1521-3773(20000417)39:8<1458::AID-ANIE1458>3.0.CO
[9]  
2-E
[10]  
Aratani N., 2000, ANGEW CHEM, V112, P1517