Issue 32, 2005
From the journal:

Chemical Communications

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

Daniel L. Reger,*a   J. Derek Elgin,a   Radu F. Semeniuc,a   Perry J. Pellechiaa  and  Mark D. Smitha  

* Corresponding authors

a University of South Carolina, Department of Chemistry and Biochemistry, 631 Sumter Street, Columbia, SC 29208, USA
E-mail: Reger@mail.chem.sc.edu
Fax: +1 (803)777-9521
Tel: +1 (803)777-2587

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, PGSE–NMR 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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Article information

DOI
https://doi.org/10.1039/B504998A
Article type
Communication
Submitted
11 Apr 2005
Accepted
21 Jun 2005
First published
14 Jul 2005

Chem. Commun., 2005, 4068-4070

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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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