Ravikanth, M. ; Strachan, Jon-Paul ; Li, Feirong ; Lindsey, Jonathan S. (1998) Trans-substituted porphyrin building blocks bearing iodo and ethynyl groups for applications in bioorganic and materials chemistry Tetrahedron, 54 (27). pp. 7721-7734. ISSN 0040-4020
Full text not available from this repository.
Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/S0040-4020(98)00408-6
Abstract
The modular synthesis of linear or cyclic multiporphyrin arrays relies on the availability of trans-substituted porphyrin building blocks with high solubility in organic solvents. Eleven porphyrin building blocks were synthesized bearing iodo, ethynyl and 2-(trimethylsilyl)ethynyl groups at the 4-, 3- or 3,5-positions of two meso-aryl units and mesityl groups at the other two meso-positions. The synthesis involves condensation of 5-mesityldipyrromethane with one or two aryl aldehydes. Combinations of functional groups include di-iodo, tetra-iodo, bis[(2-(trimethylsilyl)ethynyl], iodo and 2-(trimethylsilyl)ethynyl and ethynyl and 2-(trimethylsilyl)ethynyl. In addition, a porphyrin bearing one 4-iodophenyl group and one 3,5-bis(boron-dipyrrin)phenyl group was synthesized for applications in molecular photonic devices. The iodo and ethynyl groups are ideally-suited for Pd-mediated coupling reactions, allowing the porphyrin building blocks to be joined in the systematic construction of soluble multiporphyrin arrays.
Item Type: | Article |
---|---|
Source: | Copyright of this article belongs to Elsevier Science. |
ID Code: | 104506 |
Deposited On: | 30 Nov 2017 12:35 |
Last Modified: | 30 Nov 2017 12:35 |
Repository Staff Only: item control page