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Coordination Ability of Ligand Containing Electron Rich Phosphorous Nitrogen or Chelcogen Centers towards Transition Metals

机译：含电子富集氮或化学原的配体与过渡金属的配位能力

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Chauhan Abhai Jeet;
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年度 1989
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正文语种 en
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1. Transition Metal Complexes with Sulfur Ligands, 143 Coordination of CO, NO, N_2H_2, and Other Nitrogenase Relevant Small Molecules to Sulfur-Rich Ruthenium Complexes with the New Ligand 'tpS_4'~(2-) = 1,2-Bis(2-mercaptophenylthio) phenylene(2-) [J] . Dieter Sellmann, Klaus Engl, Frank W. Heinemann, European journal of inorganic chemistry . 2000,第5期

机译：含硫配体的过渡金属配合物，CO，NO，N_2H_2和其他与固氮酶相关的小分子与新配体'tpS_4'〜（2-）= 1,2-2-双（2-巯基苯硫基）的富硫钌配合物的143配位）亚苯基（2-）
2. Transition metal complexes with sulfur ligands. 136. Enforced trans coordination of thiolate donors in electron rich iron, ruthenium, and nickel [M(L)(pyN(2)H(2)S(2))] and [M(L)(pyS(4))] complexes (L = CO, PPh3, DMSO) (pyN(2)H(2)S(2)(2-)=2,6-bis(2-me [J] . Sellmann D., Heinemann FW., Utz J. Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics . 1999,第23期

机译：具有硫配体的过渡金属配合物。 136.富电子的铁，钌和镍中的硫醇盐供体的反式配位[M（L）（pyN（2）H（2）S（2））]和[M（L）（pyS（4））]配合物（L = CO，PPh3，DMSO）（pyN（2）H（2）S（2）（2-）= 2,6-bis（2-me
3. A unified understanding of the direct coordination of NO to first-transition-row metal centers in metal-ligand complexes [J] . Lee Hyunjoo, Kang Joongoo Physical chemistry chemical physics: PCCP . 2017,第41期

机译：对金属配体复合物中NO直接转换排金属中心的直接协调的统一理解
4. Synthesis and investigation of energetic transition metal complexes using di(1H-tetrazol-5-yl)methane as nitrogen-rich ligand [C] . Thomas M. Klapoetke, Joerg Stierstorfer, Norbert Szimhardt Seminar on New Trends in Research of Energetic Materials . 2015

机译：以二（1H-四唑-5-基）甲烷为富氮配体的高能过渡金属配合物的合成与研究
5. Mechanisms of electron transfer and hydrogen activation in selected triruthenium clusters with multiple bridging ligands. Part I. The attenuation of radical reactivity in triruthenium trihydrido(alkylidyne) clusters. Electrochemistry and kinetics of decomposition of the 47-electron cluster radical, via a disproportionation path. Part II. The activation of molecular hydrogen at transition metal centers via kinetics and mechanism of reversible oxidative addition of hydrogen across the metal-metal bond of (mu-hydrogen)(2)Ruthenium(3)(Carbon monoxide)(8)(mu-phosphorus(t-BU)(2))(2). [D] . Bierdeman, David John. 2000

机译：具有多个桥联配体的选定三钌簇中电子转移和氢活化的机理。第一部分。三氢三钌（亚烷基）簇中自由基反应性的减弱。通过歧化路径分解47电子簇自由基的电化学和动力学。第二部分通过（mu-hydrogen）（2）钌（3）（一氧化碳）（8）（mu-phosphorus（）的金属-金属键上氢的可逆氧化加成反应的动力学和机理激活过渡金属中心的分子氢t-BU）（2））（2）。
6. Stable Cyclic (Alkyl)(Amino)Carbenes as Rigid or Flexible Bulky Electron-Rich Ligands for Transition-Metal Catalysts: A Quaternary Carbon Atom Makes the Difference [O] . Vincent Lavallo, Yves Canac, Carsten Präsang, -1

机译：稳定的环状（烷基）（氨基）碳烯用作过渡金属催化剂的刚性或柔性大体积电子富集配体：季碳原子有所作为
7. Studies on the Coordination Compounds of Transition Metals Containing Ligands of Electron Rich Elements [O] . Bashar Abdul 1990

机译：含富电子元素配体的过渡金属配位化合物的研究

Coordination Ability of Ligand Containing Electron Rich Phosphorous Nitrogen or Chelcogen Centers towards Transition Metals

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