Faculty Opinions recommendation of [FeFe]-hydrogenase cyanide ligands derived from S-adenosylmethionine-dependent cleavage of tyrosine.

2010 ◽  
Author(s):  
Wolfgang Buckel
Keyword(s):  
Cyanide Ligands

Synthesis and crystal structures of bis(imidazolidine-2-thione-κS)bis(thiocyanato-κS)mercury(II) and bis(cyanido)bis(μ2-imidazolidine-2-thione-κS)mercury(II).Hg(CN)2

2017 ◽  
Vol 72 (9) ◽  
pp. 671-676 ◽  
Author(s):  
Muhammad Ashraf Shaheen ◽  
Muhammad Nawaz Tahir ◽  
Sarwat Sabir ◽  
Aneela Anwar ◽  
Anvarhusein A. Isab ◽  
...  
Keyword(s):  
Rotation Axis ◽  
Mercury Atom ◽  
Distorted Octahedral Geometry ◽  
Weakly Bound ◽  
X Ray ◽  
X Ray Crystallography ◽  
Hydrogen Bonding Interactions ◽  
Ir And Nmr Spectroscopy ◽  
Distorted Octahedral ◽  
Cyanide Ligands

AbstractTwo mercury(II) complexes containing imidazolidine-2-thione (Imt) and thiocyanate or cyanide ligands, [Hg(Imt)2(SCN)2] (1) and [Hg(Imt)2(CN)2].Hg(CN)2(2), have been prepared and characterized by IR and NMR spectroscopy and X-ray crystallography. In compound1, the mercury atom is located on a two-fold rotation axis and is coordinated to two thione sulfur atoms of imidazolidine-2-thione (Imt) and to two sulfur atoms of thiocyanate in a distorted tetrahedral mode with the S-Hg-S bond angles in the range of 98.96(3)–148.65(6)°. In2, the mercury atom is hexa-coordinated having a distorted octahedral geometry composed of two cyanide C atoms [Hg-C=2.055(5) Å] and four weakly bound thione S atoms of imidazolidine-2-thione (Imt) [Hg-S=3.1301(13) and 3.1280(13) Å]. One free Hg(CN)2molecule is also present in the crystal. In both complexes, the molecular structure is stabilized by N-H…N and N-H…S hydrogen bonding interactions.

Cyano-Bridged Bimetallic Complexes of Copper(II) with Nitroprusside. Crystal Structure of [Cu(H2NCH2CH(NH2)CH3)2Fe(CN)5NO] . H2O

2000 ◽  
Vol 53 (3) ◽  
pp. 225 ◽  
Author(s):  
Zdenek Smékal ◽  
Zdenek Trávnícek ◽  
Jaromír Marek ◽  
Milan Nádvornik
Keyword(s):  
Crystal Structure ◽  
Structural Analysis ◽  
Magnetic Measurements ◽  
X Ray ◽  
Cyanide Group ◽  
Cyanide Ligand ◽  
Binuclear Structure ◽  
Tetragonal Pyramidal ◽  
Cyanide Ligands ◽  
Diamine Ligands

Five new complexes of compositions [Cu(1,2-pn)2Fe(CN)5NO]·H2O (1,2-pn = propane-1,2-diamine) and [Cu(L)Fe(CN)5NO]·xH2O (L = tmen (N,N,N′,N′-tetramethylethane-1,2-diamine), x = 0.5; L = trimeen (N,N,N′-trimethylethane-1,2-diamine), x = 1; L = dien (N-(2-aminoethyl)ethane-1,2-diamine), x = 0; L = medpt (N-(3-aminopropyl)-N-methylpropane-1,3-diamine), x = 2) have been isolated from the reaction mixture of Cu(ClO4)2·6H2O (or CuCl2·2H2O), the amine and Na2 [Fe(CN)5NO]·2H2O in water. The complexes have been characterized by infrared and ultraviolet–visible spectroscopies, and magnetic measurements. Single-crystal X-ray structural analysis revealed that the [Cu(1,2-pn)2Fe(CN)5NO]·H2O complex assumes a cyanide-bridged binuclear structure in which iron(II) is six-coordinated by five cyanide ligands and one nitrosyl group (the nitrosyl group lies cis to the bridging cyanide group), while copper(II) is five-coordinated by two propane-1,2-diamine ligands and a bridging cyanide ligand in a distorted tetragonal pyramidal arrangement.

Dimethylplatinum(IV) Complexes With Cyanide: Thermal and Photoassisted Substitution Reactions, and Characterization of Products by N.M.R.

1987 ◽  
Vol 40 (9) ◽  
pp. 1565 ◽  
Author(s):  
TG Appleton ◽  
JR Hall ◽  
MA Williams
Keyword(s):  
Ultraviolet Irradiation ◽  
Oxidative Addition ◽  
Reductive Elimination ◽  
Methyl Groups ◽  
Substitution Reactions ◽  
Aqueous Acid ◽  
Cyanide Ligands ◽  
Cis And Trans ◽  
Insoluble Precipitate

Reactions of cyanide with the dimethylplatinum (IV) complexes, [PtMe2(OH) (H20)1.5 n, [PtMe2Br2]n and fac-PtMe2Br(H2O)3+, have been studied, principally by 1H, 13C and 195Pt n.m.r. Cyanide rapidly displaces the ligands trans to the methyl groups. Subsequent reactions cis to the methyl groups occur more slowly with heating, or, for bromo complexes, on ultraviolet irradiation. These substitution reactions compete with reductive elimination of groups from the platinum(IV) compounds to produce platinum(II) products. All attempts to prepare solutions of fac-PtMe2(CN)(H2O)3+ were unsuccessful. Oxidative addition of ICN to cis-PtMe2( py )2 ( py = pyridine) gave PtMe2I(CN)( py )2, from which a solution of fac-PtMe2(CN)( MeOH )3+ in methanol could be obtained. Addition of water or aqueous acid to this solution gave a very insoluble precipitate of [PtMe2(CN)(OH)n. The cis and trans influences on Jpt -C and δC of the cyanide ligands have been evaluated.

A New One-Dimensional Bimetallic Complex: Cu(en)2Fe(CN)5(NO). Synthesis, Crystal Structure and Magnetic Behaviour

1998 ◽  
Vol 51 (8) ◽  
pp. 661 ◽  
Author(s):  
Hui-Zhong Kou ◽  
Hong-Mei Wang ◽  
Dai-Zheng Liao ◽  
Peng Cheng ◽  
Zong-Hui Jiang ◽  
...  
Keyword(s):  
Copper Complexes ◽  
Bond Distance ◽  
Chain Structure ◽  
Magnetic Behaviour ◽  
Teller Distortion ◽  
Magnetic Investigation ◽  
Jahn Teller ◽  
Cyanide Ligands ◽  
Jahn Teller Distortion ◽  
Shed Light

The nitrosyl cyanide Cu(en)2Fe(CN)5(NO) was prepared by the reaction of Cu(en)2Cl2 and Na2 [Fe(CN)5(NO)].2H2O in aqueous solution. Single-crystal X-ray structure analysis revealed that the complex assumes a cyanide-bridged chain structure in which iron(II) is coordinated by five cyanide ligands and a nitrosyl group, and copper(II) is coordinated by two ethylenediamine ligands and two bridging cyanide ligands. The copper centres display a typical Jahn–Teller distortion characteristic of octahedral copper complexes with bond distance deviations in lattice symmetry from octahedral ideality: Cu-N(equatorial, mean) 2·010(3) Å and Cu-N(axial, mean) 2·569(3) Å. Infrared and ultraviolet studies shed light on the above molecular structure. A magnetic investigation showed the presence of a weak antiferromagnetic interaction (J = -1·06 cm-1) between the copper atoms within each chain through the diamagnetic Fe(CN)5(NO)2- ions.

Functionalization of [Re6Q8(CN)6]4− clusters by methylation of cyanide ligands

2019 ◽  
Vol 43 (41) ◽  
pp. 16338-16348 ◽  
Author(s):  
Maksim A. Mikhaylov ◽  
Alina D. Mironova ◽  
Konstantin A. Brylev ◽  
Taisiya S. Sukhikh ◽  
Ilia V. Eltsov ◽  
...  
Keyword(s):  
Cluster Complexes ◽  
Cyanide Ligands ◽  
Anionic Cluster

Methylation of anionic cluster complexes [Re6Q8(CN)6]4− with ((CH3)3O)BF4 or CF3SO3CH3 afforded homoleptic isonitrile cluster complexes [Re6Q8(CH3NC)6]2+ (Q = S, Se, Te).

Synthesis, structure, luminescence and magnetic properties of the coordination polymer {[Eu(H2O)5][Mo(CN)8]}∞ containing bridging cyanide ligands

2010 ◽  
Vol 59 (2) ◽  
pp. 476-479 ◽  
Author(s):  
E. N. Chelebaeva ◽  
A. A. Trifonov ◽  
J. E. Larionova ◽  
Y. Guari ◽  
R. A. Sa Fereira ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Coordination Polymer ◽  
Cyanide Ligands

Synthesis, Crystal Structure and Magnetic Properties of Novel Complex [μ-(NC)-Fe(CN)3(NO)-μ-(CN)-Cu(ept)]n·4nH2O (ept = N-(2-Aminoethyl)propane-1,3-diamine)

2001 ◽  
Vol 66 (10) ◽  
pp. 1490-1498 ◽  
Author(s):  
Zdeněk Smékal ◽  
Jiří Kameníček ◽  
Ingrid Svoboda ◽  
Albert Escuer
Keyword(s):  
Crystal Structure ◽  
Magnetic Measurement ◽  
Antiferromagnetic Interaction ◽  
Title Complex ◽  
The Novel ◽  
One Dimensional ◽  
X Ray ◽  
Magnetic Investigation ◽  
Novel Complex ◽  
Cyanide Ligands

The novel complex [μ-(NC)-Fe(CN)3(NO)-μ-(CN)-Cu(ept)]n·4nH2O (ept = N-(2-aminoethyl)- propane-1,3-diamine) was obtained by the reaction of Cu(ClO4)2·6H2O with N-(2-amino- ethyl)propane-1,3-diamine and Na2[Fe(CN)5NO]·2H2O in water. This compound was characterized by IR, UV-VIS and EPR spectroscopies and magnetic measurement. Single-crystal X-ray structure analysis revealed that the title complex has a one-dimensional polymeric structure containing hexacoordinate iron(II) with five cyanide ligands (two of them, in trans position, bridging) and one nitrosyl group, and pentacoordinate copper(II) with N-(2-aminoethyl)propane-1,3-diamine and two sites occupied by bridging cyanide ligands. Magnetic investigation revealed a very weak antiferromagnetic interaction between the copper atoms (superexchange interaction parameter J = -1.7(1) cm-1; H = -JSiSi+1) within the chain through the diamagnetic [Fe(CN)5NO]2- ions.

scholarly journals Crystal structure of the coordination polymer [FeIII2{PtII(CN)4}3]

2015 ◽  
Vol 71 (1) ◽  
pp. i1-i2
Author(s):  
Maksym Seredyuk ◽  
M. Carmen Muñoz ◽  
José A. Real ◽  
Turganbay S. Iskenderov
Keyword(s):  
Crystal Structure ◽  
Coordination Polymer ◽  
Point Group ◽  
Three Dimensional ◽  
Title Complex ◽  
Group Symmetry ◽  
Point Group Symmetry ◽  
Rotation Axes ◽  
Square Planar ◽  
Cyanide Ligands

The title complex, poly[dodeca-μ-cyanido-diiron(III)triplatinum(II)], [FeIII2{PtII(CN)4}3], has a three-dimensional polymeric structure. It is built-up from square-planar [PtII(CN)4]2−anions (point group symmetry 2/m) bridging cationic [FeIIIPtII(CN)4]+∞layers extending in thebcplane. The FeIIatoms of the layers are located on inversion centres and exhibit an octahedral coordination sphere defined by six N atoms of cyanide ligands, while the PtIIatoms are located on twofold rotation axes and are surrounded by four C atoms of the cyanide ligands in a square-planar coordination. The geometrical preferences of the two cations for octahedral and square-planar coordination, respectively, lead to a corrugated organisation of the layers. The distance between neighbouring [FeIIIPtII(CN)4]+∞layers corresponds to the lengtha/2 = 8.0070 (3) Å, and the separation between two neighbouring PtIIatoms of the bridging [PtII(CN)4]2−groups corresponds to the length of thecaxis [7.5720 (2) Å]. The structure is porous with accessible voids of 390 Å3per unit cell.

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