Issue 3, 1993

Self-assembly of a bisporphyrin supramolecular cage induced by molecular recognition between complementary hydrogen bonding sites

Abstract

Addition of an alkyl substituted triaminopyrimidine, TAP, to a solution of porphyrin 2 bearing two rigidly attached complementary hydrogen bonding moieties of the uracil type, leads to the self-assembly of a bisporphyrin supramolecular cage structure 1 from the syn rotamer and probably a zig-zag strand from the anti rotamer.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 243-245

Self-assembly of a bisporphyrin supramolecular cage induced by molecular recognition between complementary hydrogen bonding sites

C. M. Drain, R. Fischer, E. G. Nolen and J. Lehn, J. Chem. Soc., Chem. Commun., 1993, 243 DOI: 10.1039/C39930000243

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements