Cyclopentadienylruthenium π Complexes of Subphthalocyanines: A "Drop-Pin" Approach To Modifying the Electronic Features of Aromatic Macrocycles

被引:43
作者
Caballero, Esmeralda [1 ]
Fernandez-Ariza, Javier [1 ]
Lynch, Vincent M. [2 ,3 ]
Romero-Nieto, Carlos [4 ,5 ]
Salome Rodriguez-Morgade, M. [1 ]
Sessler, Jonathan L. [2 ,3 ]
Guldi, Dirk M. [4 ,5 ]
Torres, Tomas [1 ,6 ]
机构
[1] Univ Autonoma Madrid, Dept Quim Organ, E-28049 Madrid, Spain
[2] Univ Texas Austin, Dept Chem & Biochem, Austin, TX 78712 USA
[3] Univ Texas Austin, Inst Cellular & Mol Biol, Austin, TX 78712 USA
[4] Univ Erlangen Nurnberg, Dept Chem & Pharm, D-91058 Erlangen, Germany
[5] Univ Erlangen Nurnberg, ICMM, D-91058 Erlangen, Germany
[6] IMDEA Nanociencia, Madrid 28049, Spain
基金
美国国家科学基金会;
关键词
arene ligands; pi complexes; ruthenium; subphthalocyanines; subporphyrazines; PHOTOINDUCED CHARGE-TRANSFER; ENERGY-TRANSFER; METALLOPORPHYRINS; SUBPORPHYRINS; NONPLANAR; VERSATILE;
D O I
10.1002/anie.201206111
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Facing facts: Coordination of Cp*Ru (Cp*=C5Me 5) to the concave and convex π surfaces of subphthalocyanines constitutes a new approach to the functionalization of subazaporphyrins. While the convex face shows higher reactivity, coordination to the concave side produces a stronger diatropic influence on the Cp* ligand and a greater perturbation of the macrocyclic π-electronic features. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
收藏
页码:11337 / 11342
页数:6
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