| Literature DB >> 25703370 |
Hua-Tang Cai1, Qian-Ting Liu1, Hui-Qing Ye1, Li-Jie Su1, Xiao-Xu Zheng1, Jin-Ni Li1, Shu-Hua Ou1, Jia-Rong Zhou2, Le-Min Yang1, Chun-Lin Ni3.
Abstract
The reaction of CoCl2 with the naphthalene methylated triphenylphosphinium bromide [n-NAPMeTPP]Br (n=1, 2) and KSCN, in a methanolic medium at ambient temperature, leads to the self-assembly formation of hybrid 2:1 organic-inorganic molecular solids, [1-NAPMeTPP]2[Co(NCS)4](1) and [2-NAPMeTPP]2[Co(NCS)4](2) ([NAPMeTPP](+)=(naphthylmethylene)(triphenyl)phosphinium), which have been characterized by elemental analyses, IR spectroscopy, UV-Vis spectra, ESI-MS, molar conductivity and single-crystal X-ray diffraction structural analyses. Compound 1 crystallizes in the orthorhombic space group Pna21, while 2 does in the monoclinic space group C2/c. The cations form a dimer through the weak intermolecular C-H⋯π interactions in 1 and π⋯π interaction in 2, while the anion and cation are linked by the C-H⋯S hydrogen bond in 1. Two molecular solids show dual functionalities: (1) the broad fluorescence emission around 400nm in the solid state at room temperature; (2) the weak antiferromagnetic coupling behavior.Entities:
Keywords: Crystal structure; Fluorescence; Magnetic properties; Naphthalene methylated triphenylphosphinium; Tetra(isothiocyanate)cobal(II) dianion
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Year: 2015 PMID: 25703370 DOI: 10.1016/j.saa.2015.01.098
Source DB: PubMed Journal: Spectrochim Acta A Mol Biomol Spectrosc ISSN: 1386-1425 Impact factor: 4.098