Crystal structures of copper(I) and silver(I) chloride complexes containing 4-phenylthiosemicarbazide and triphenylphosphine ligands

被引:5
|
作者
Wattanakanjana, Yupa [1 ]
Janwatthana, Kamonwan [1 ]
Romyen, Tanaporn [1 ]
Nimthong-Roldan, Arunpatcha [2 ]
机构
[1] Prince Songkla Univ, Fac Sci, Div Phys Sci, Hat Yai 90112, Thailand
[2] Predev Sci, 211,2nd Ave, Waltham, MA 02451 USA
来源
SCIENCEASIA | 2021年 / 47卷
基金
美国国家科学基金会;
关键词
silver(I) chloride; copper(I) chloride; 4-phenylthiosemicarbazide; crystal structure; intra- and intermolecular hydrogen bonding; THIOSEMICARBAZIDES; HYBRIDS;
D O I
10.2306/scienceasia1513-1874.2021.S001
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Copper(I) and silver(I) chloride complexes containing triphenylphosphine (PPh3) and 4-phenyl-thiosemicarbazide (4-PTSC) ligands were prepared and structurally analyzed, namely [CuCl(4-PTSC)(PPh3)(2)] (1) and [AgCl(4-PTSC)(PPh3)(2)]CH3CN (2). Both compounds (1) and (2) exhibit a distorted tetrahedral metal coordination environment with two P atoms from two PPh3 ligands, one terminal S atom from the 4-PTSC ligand and a chloride ion. Intramolecular N-H center dot center dot center dot Cl and N-H center dot center dot center dot N hydrogen bonds are observed (graph set motifs S (6) and S (5), respectively). In the crystals of both complexes, molecules are linked to form dimers via bifurcated N-H center dot center dot center dot Cl hydrogen bonds involving the amine and chloride units. For compound (2), a solvate acetonitrile molecule acts as a hydrogen bond donor and acceptor via C-H(CH3CN) center dot center dot center dot Cl and C-H center dot center dot center dot N(CH3CN) interactions, leading to the formation of 1D chains along [010].
引用
收藏
页码:28 / 33
页数:6
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