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Synthesis, structural characterization and DFT calculations of a diphenyl-2-pyridylphosphine complex of copper(II)
被引:0
|作者:
Nath, Jayashree
[1
]
Guha, Ankur Kanti
[2
]
Edelmann, Frank T.
[3
]
Sarma, Bipul
[4
]
Sarmah, Bhaskar Jyoti
[5
]
机构:
[1] JB Coll, Dept Chem, Jorhat, Assam, India
[2] Cotton Univ, Dept Chem, Gauhati, Assam, India
[3] Otto von Guericke Univ, Chem Inst, Magdeburg, Germany
[4] Tezpur Univ, Dept Chem Sci, Napam, Assam, India
[5] Jorhat Inst Sci & Technol, Dept Chem, Jorhat, Assam, India
关键词:
Phosphine ligand;
chelate ring expansion;
DFT study;
SUPPORTED ORGANOMETALLIC COMPLEXES;
COORDINATION-COMPOUNDS;
DIAMINE(ETHER-PHOSPHINE)RUTHENIUM(II) COMPLEXES;
CATALYTIC-HYDROGENATION;
PHOSPHINE-LIGANDS;
ACID;
POLYMERIZATION;
CARBONYLATION;
DIVERSITY;
DRIVEN;
D O I:
10.1080/00958972.2023.2276053
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
The reaction of Cu(NO3)(2)<middle dot>3H(2)O with a potentially bidentate P,N-donor ligand, diphenyl-2-pyridylphosphine (PPh2Py), in 1:2 molar ratio resulted in formation of a kappa N-2,O-chelated complex, [Cu(kappa N-2,O-P(O)Ph2Py)(2)(NO3)(2)] (1). A single-crystal X-ray study confirmed the formation of a five-membered kappa N-2, O-chelate involving pyridyl nitrogen and phosphine oxide oxygen donor sites. A DFT study was carried out on 1 to understand the chelate ring expansion process upon oxidation with PPh2Py. DFT analysis revealed that 1 contains a relatively strong M-N bond compared to its M-P bond, facilitating the oxidation of the P atom followed by chelate ring expansion.
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页码:1867 / 1878
页数:12
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