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Updated: May 4, 2026

Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of PhosphorusI
Published on: November 22, 2016
Bis[O,O'-bis-(4-tert-butyl-phen-yl) di-thio-phosphato-κ(2) S,S']bis-(pyridine-κN)lead(II)
Xiulan Zhang1, Bin Xie1, Linxin He2
1Institute of Functionalized Materials, Sichuan University of Science and Engineering, Zigong 643000, People's Republic of China ; College of Chemistry and Pharmaceutical Engineering, Sichuan University of Science and Engineering, Zigong 643000, People's Republic of China.
Abstract:
In the title compound, [Pb(C20H26O2PS2)2(C5H5N)2], the Pb(II) ion is coordinated by two S,S'-bidentate anions and two pyridine mol-ecules. The PbN2S4 coordination geometry approximates to a penta-gonal bipyramid with one equatorial site vacant. The N atoms occupy the axial sites. One of the pyridine mol-ecules is disordered over two sets of sites in a 0.907 (7):0.093 (7) ratio and one of the tert-butyl groups is disordered over two sets of sites in a 0.534 (6):0.466 (6) ratio. An intra-molecular C-H⋯O inter-action occurs in one of the ligands. In the crystal, pairs of short Pb⋯S contacts [3.4018 (11) Å] generate a centrosymmetric dimeric assembly with the distant S atom lying in the region of the vacant coordination site of the metal atom. No directional packing inter-actions occur.
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