نتایج جستجو برای: coordination solvent

تعداد نتایج: 132304  

2014
Eduard N. Chygorin Yuri O. Smal Vladimir N. Kokozay Irina V. Omelchenko

The title cluster, [Cu4(C11H12N2O6)4], was obtained from the Cu(0)-FeCl2·4H2O-H4 L-Et3N-DMF reaction system (in air), where H4 L is 2-hy-droxy-methyl-2{[(2-hy-droxy-3-nitro-phen-yl)methyl-idene]amino}-propane-1,3-diol and DMF is di-methyl-formamide. The asymmetric unit consists of one Cu(2+) ion and one dianionic ligand; a -4 symmetry element generates the cluster, which contains a {Cu4O4} cuba...

2011
Kwang Ha

The asymmetric unit of the title compound, [Mn(C(8)H(6)N(4))(2)(H(2)O)(2)](ClO(4))(2)·2CH(3)NO(2)·H(2)O, contains one half of a cationic Mn(II) complex, a ClO(4) (-) anion, a nitro-methane solvent mol-ecule and one half-mol-ecule of water. The complex mol-ecule and the solvent water mol-ecule are located on a twofold rotation axis. In the complex, the Mn(II) ion has a distorted cis-N(4)O(2) oct...

2011
Shi-Juan Wang Kai-Long Zhong

In the title compound, [Co(SO(4))(C(12)H(8)N(2))(2)]·C(4)H(10)O(2), the Co(2+) ion has a distorted octa-hedral coordination environment composed of four N atoms from two chelating 1,10-phenanthroline ligands and two O atoms from an O,O'-bidentate sulfate anion. The dihedral angle between the two chelating N(2)C(2) groups is 83.48 (1)°. The Co(2+) ion, the S atom and the mid-point of the central...

2012
Maryke Steyn Hendrik G. Visser Andreas Roodt

In the title compound, [Zr(C(11)H(10)NO)(4)]·2C(3)H(7)NO, the Zr(IV) ion is coordinated by four bidentate 5,7-dimethylquinolin-8-olate ligands in a slightly distorted square-anti-prismatic coordination environment. The asymmetric unit also contains two N,N'-dimethyl-formamide (DMF) solvent mol-ecules. In the crystal, a weak C-H⋯O hydrogen bond links the complex mol-ecule to a solvent mol-ecule ...

2016
Tim B van Driel Kasper S Kjær Robert W Hartsock Asmus O Dohn Tobias Harlang Matthieu Chollet Morten Christensen Wojciech Gawelda Niels E Henriksen Jong Goo Kim Kristoffer Haldrup Kyung Hwan Kim Hyotcherl Ihee Jeongho Kim Henrik Lemke Zheng Sun Villy Sundström Wenkai Zhang Diling Zhu Klaus B Møller Martin M Nielsen Kelly J Gaffney

The interactions between the reactive excited state of molecular photocatalysts and surrounding solvent dictate reaction mechanisms and pathways, but are not readily accessible to conventional optical spectroscopic techniques. Here we report an investigation of the structural and solvation dynamics following excitation of a model photocatalytic molecular system [Ir2(dimen)4]2+, where dimen is p...

Journal: :Nature chemistry 2017
Isaak Unger Robert Seidel Stephan Thürmer Marvin N Pohl Emad F Aziz Lorenz S Cederbaum Eva Muchová Petr Slavíček Bernd Winter Nikolai V Kryzhevoi

Photoionization is at the heart of X-ray photoelectron spectroscopy (XPS), which gives access to important information on a sample's local chemical environment. Local and non-local electronic decay after photoionization-in which the refilling of core holes results in electron emission from either the initially ionized species or a neighbour, respectively-have been well studied. However, electro...

Journal: :Applied Magnetic Resonance 2021

Abstract The photo-excited triplet state of Zn-protoporphyrin IX located in the heme pocket human neuroglobin has been investigated by time-resolved EPR coupled to magnetophotoselection. protein matrix compared with model complex organic glass, considering both non-coordinating and coordinating solvent mixtures. plays an important role stabilizing coordination embedded chromophore, resulting a ...

2012
Haleden Chiririwa Alfred Muller

The crystal structure of the title compound, [PtCl(2)(C(25)H(22)NPS)]·0.5CH(2)Cl(2), was determined to establish the coordination properties of the (phosphan-yl)benzyl-idene-methanamine ligand to platinum. In the unit cell two mol-ecules of cis-[PtCl(2)(C(25)H(22)NPS)] are accompanied by a dichloro-methane solvent mol-ecule. The square-planar Pt(2+) coordination sphere is slightly distorted wit...

2015
Albert Poater Luigi Cavallo

During a Ru-catalyzed reaction of an olefin with an alkylidene moiety that leads to a metallacycle intermediate, the cis insertion of the olefin can occur from two different directions, namely side and bottom with respect to the phosphine or N-heterocyclic ligand (NHC), depending on the first or second generation Grubbs catalyst. Here, DFT calculations unravel to which extent the bottom coordin...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید