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Issue 32, 2005
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Directional control of π-stacked building blocks for crystal engineering: the 1,8-naphthalimide synthon

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Abstract

Incorporating the 1,8-naphthalimide group into bis(pyrazolyl)methane ligands triggers the association of their rhenium(I) complexes into directionally ordered dimers in both solution and solid state, as demonstrated by ES+/MS, PGSENMR and X-ray diffraction studies.

Graphical abstract: Directional control of π-stacked building blocks for crystal engineering: the 1,8-naphthalimide synthon

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Supplementary files

Article information


Submitted
11 Apr 2005
Accepted
21 Jun 2005
First published
14 Jul 2005

Chem. Commun., 2005, 4068-4070
Article type
Communication

Directional control of π-stacked building blocks for crystal engineering: the 1,8-naphthalimide synthon

D. L. Reger, J. D. Elgin, R. F. Semeniuc, P. J. Pellechia and M. D. Smith, Chem. Commun., 2005, 4068
DOI: 10.1039/B504998A

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