Macrocyclic Platinum(II) Complexes with a Bifunctional Diphosphine Ligand
作者:Andrea E. Pascui、Karlotta van Rees、Dirk W. Zant、Daniël L. J. Broere、Maxime A. Siegler、Jarl Ivar van der Vlugt
DOI:10.1002/ejic.201501055
日期:2015.12
cis-PtCl2(1H2) (2), or the kinetic trans isomer, trans-PtCl2(1H2) (3). Both species have been fully characterized both in the solid state and in solution. Thermodynamic parameters for isomerization processes of 2 and 3 have been determined. Halide abstraction from 2 and 3 led to formation of cis-[Pt(CH3CN)(Cl)(1H2)]BF4 and trans-[Pt(CH3CN)(Cl)(1H2)]BF4.
Sterically and Electronically Flexible Pyridylidene Amine Dinitrogen Ligands at Palladium: Hemilabile
<i>cis</i>
/
<i>trans</i>
Coordination and Application in Dehydrogenation Catalysis
作者:Nicolas Lentz、Yanik Streit、Pascal Knörr、Martin Albrecht
DOI:10.1002/chem.202202672
日期:2022.12.6
A new N,N,N-pyridylidene–amine (PYE) was synthesized, and its coordination to palladium was investigated. A flexible and hemilabile behavior of the ligand was put in light in terms of donation properties (zwitterionic vs. neutral) and in terms of geometry (cis/trans coordination). The complexes were found to catalytically dehydrogenate formic acid in CO2 and H2 in a state-of-the-art activity.
合成了一种新的N , N , N-亚吡啶胺 (PYE) ,并研究了它与钯的配位。根据捐赠特性(两性离子与中性)和几何形状(顺式/反式配位),阐明了配体的灵活和半稳定行为。发现这些络合物以最先进的活性在 CO 2和 H 2中催化脱氢甲酸。
<b>Aromatic and Pseudoaromatic Non-benzenoid Systems. III. The Synthesis of Some Ten π-Electron Systems<sup>1-3</sup></b>
作者:Norman L. Allinger、Gilbert A. Youngdale
DOI:10.1021/ja00865a030
日期:1962.3
426. Internuclear cyclisation. Part V. The cyclisation of derivatives of diphenylmethane, benzophenone, and N-methyldiphenylamine
作者:D. H. Hey、R. D. Mulley
DOI:10.1039/jr9520002276
日期:——
WILSHIRE, JOHN F. K., AUSTRAL. J. CHEM., 41,(1988) N 6, C. 995-1001