NMR investigations on a series of diplatinum (II) complexes possessing phenylpropenoids in CDCl3 and CD3CN: Crystal structure of a mononuclear platinum complex

Polyhedron ◽  
2021 ◽  
pp. 115612
Author(s):  
Pham Van Thong ◽  
Nguyen Thi Thanh Chi ◽  
Mohammad Azam ◽  
Cu Hong Hanh ◽  
Le Thi Hong Hai ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Platinum Complex

scholarly journals The Crystal Structure and Absolute Configuration of the Antitumor Platinum Complex tran(OH)-Pt(OH)2(Malonato)(1R, 2R, -Cyclohexanediamine)

1992 ◽  
Vol 40 (4) ◽  
pp. 1022-1024 ◽  
Author(s):  
Masafumi GOTO ◽  
Junzo HIROSE ◽  
Masahide NOJI ◽  
Keun-Im LEE ◽  
Reiko SAITO ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Absolute Configuration ◽  
Platinum Complex

scholarly journals Rigid and concave, 2,4-cis-substituted azetidine derivatives: A platform for asymmetric catalysis

2018 ◽  
Author(s):  
Akina Yoshizawa ◽  
Antonio Feula ◽  
Louise Male ◽  
Andrew G. Leach ◽  
John Fossey
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Asymmetric Catalysis ◽  
Enantiomeric Excess ◽  
Platinum Complex ◽  
Crystal Structure Analysis ◽  
Single Crystal Structure ◽  
Complex Catalyst ◽  
Reaction Conditions ◽  
Absolute Stereochemistry

A series of single enantiomer, 2,4-<i>cis</i>-disubstituted amino azetidines were synthesised and used as ligands for copper-catalysed Henry reactions of aldehydes with nitromethane. Optimisation of ligand substituents and the reaction conditions was conducted. The enantiomeric excess of the formed products was highest when alkyl aldehydes were employed in the reaction (>99% e.e.). The absolute stereochemistry of one representative azetidine derivative salt was determined by analysis of the Flack parameter of an XRD single crystal structure. The origin of selectivity in catalysis was investigated computationally, revealing the importance of the amino-substituent in determining the stereochemical outcome. A racemic platinum complex of a <i>cis</i>-disubstituted azetidine is examined by XRD single crystal structure analysis with reference to its steric parameters, and analogies to the computationally determined copper complex catalyst are drawn.<br>

Novel crystal structure of a tetranuclear platinum complex: bis(.mu.4-carbonato-O,O,O',O')-tetrakis(diammineplatinum(II)) tetranitrate trihydrate

1993 ◽  
Vol 32 (22) ◽  
pp. 4976-4978 ◽  
Author(s):  
Hans K. Mahtani ◽  
Shih Chi Chang ◽  
John R. Ruble ◽  
Iona N. L. Black ◽  
Paul B. Stein
Keyword(s):  
Crystal Structure ◽  
Platinum Complex

scholarly journals Crystal structure of homodinuclear platinum complex containing a metal–metal bond bridged by hydride and phosphide ligands

2018 ◽  
Vol 74 (7) ◽  
pp. 977-980
Author(s):  
Sakina Ouis ◽  
Djamil Azzedine Rouag ◽  
Lamia Bendjeddou ◽  
Corinne Bailly
Keyword(s):  
Crystal Structure ◽  
Diethyl Ether ◽  
Title Compound ◽  
Platinum Complex ◽  
Π Interactions ◽  
Metal Bond ◽  
Square Planar ◽  
Metal Metal

In the title compound, μ-diphenylphosphido-μ-hydrido-bis[bromido(triphenylphosphane-κP)platinum(II)] diethyl ether monosolvate, [Pt2Br2(C12H10P)H(C18H15P)2]·C4H10O or [Pt2(μ-H)(μ-PPh2)Br2(PPh3)2]·(C2H5)2O, the PtII atoms are coordinated in a distorted square-planar arrangement, with one hydrido and one phosphido ligand bridging in a trans position. In the lattice, C—H...·O and C—H...π interactions are present. This complex has a total number of 32 electrons, 16 electrons for each PtII atom. One of the Br atoms is disordered over two positions in a 0.92:0.08 ratio.

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