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Tri- and hexaferrocenyl-substituted subphthalocyanines in the quest for the optimum electron donor–acceptor distances
Chemical Communications ( IF 4.9 ) Pub Date : 2017-06-29 00:00:00 , DOI: 10.1039/c7cc04726f
Javier Fernández-Ariza 1, 2, 3, 4 , Rafael M. Krick Calderón 5, 6, 7, 8 , Josefina Perles 3, 4, 9, 10, 11 , M. Salomé Rodríguez-Morgade 1, 2, 3, 4, 12 , Dirk M. Guldi 5, 6, 7, 8 , Tomás Torres 1, 2, 3, 4, 12
Affiliation  

Three and six ferrocenyl subunits have been attached to the periphery of subphthalocyanines (SubPcs). Unlike axially coordinated ferrocenes, peripherally-bonded ferrocenes have an impact on the electronic features of SubPcs, which show a 44 to 70 nm red-shift of their Q-bands. The unusually deep and narrow ferrocenyl-SubPc is able to host C60, giving rise to atypical SubPc•C60 cocrystallates, through a combination of concave–convex and convex–convex π–π interactions.

中文翻译:

寻求最佳电子给体-受体距离的三和六铁茂铁取代的亚酞菁

三个和六个二茂铁基亚基已连接到亚酞菁(SubPcs)的外围。与轴向配位的二茂铁不同,周边键合的二茂铁对SubPcs的电子特征有影响,SubPcs的电子特征显示其Q波段发生44到70 nm的红移。异常深而狭窄的二茂铁基-SubPc能够容纳C 60,通过凹-凸和凸-凸π-π相互作用的组合,产生非典型的SubPc•C 60共结晶。
更新日期:2017-07-28
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