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

Literature Information

Publication Date 2005-07-14
DOI 10.1039/B504998A
Impact Factor 6.222
Authors

Daniel L. Reger, J. Derek Elgin, Radu F. Semeniuc, Perry J. Pellechia, Mark D. Smith


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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, PGSE–NMR and X-ray diffraction studies.

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Chemical Communications

Chemical Communications
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ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry

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