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

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

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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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2005-08 (32), p.4068-4070
Hauptverfasser: Reger, Daniel L, Elgin, J Derek, Semeniuc, Radu F, Pellechia, Perry J, Smith, Mark D
Format: Artikel
Sprache:eng
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Zusammenfassung: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.
ISSN:1359-7345
1364-548X
DOI:10.1039/b504998a