Structures of plutonium coordination compounds: A review of past work, recent single crystal x-ray diffraction results, and what we’re learning about plutonium coordination chemistry

2000 ◽  
Author(s):  
M. P. Neu
Keyword(s):  
Coordination Chemistry ◽  
Single Crystal ◽  
Coordination Compounds ◽  
X Ray Diffraction ◽  
X Ray ◽  
Past Work

New Cu(II), Co(II), and Ni(II) complexes with thieno[2,3-b]pyridine and 2-methylthieno[2,3-b]pyridine as ligands: Synthesis and crystal structures

2009 ◽  
Vol 63 (3) ◽  
Author(s):  
Ján Halgaš ◽  
Viera Kolenová ◽  
Zuzana Števíková ◽  
Lucia Perašínová ◽  
Jozef Kožíšek
Keyword(s):  
Single Crystal ◽  
Diffraction Analysis ◽  
Crystal Structures ◽  
Elemental Analysis ◽  
Zinc Chloride ◽  
Coordination Compounds ◽  
Biological Activities ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir

AbstractAlthough thienopyridines attract attention because of their biological activities, they have not been used as ligands in coordination compounds. Thieno[2,3-b]pyridine was prepared by known procedures; by reduction of 2-nitrothiophene, and reaction of the resulting 2-thienyl ammonium salt with malondialdehyde tetramethylacetal in the presence of zinc chloride. The same procedure was used for the preparation of a new derivative, 2-methylthieno[2,3-b]pyridine, starting from 2-methyl-5-nitrothiophene. The thienopyridines were used in the synthesis of coordination compounds. Chlorides, isothiocyanates, acetates, and chloroacetates of copper(II), nickel(II), or cobalt(II) were used as starting salts. The prepared complexes were characterized by elemental analysis and FT IR. Structures of the four complexes were determined by single-crystal X-ray diffraction analysis.

Eindimensionale Kupfer(II)-Koordinationspolymere: Kristall-Engineering durch variable Verknüpfungsmuster [1] / One Dimensional Copper(II) Coordination Polymers: Crystal Engineering through Variable Types of Linkage [1]

1997 ◽  
Vol 52 (1) ◽  
pp. 125-134 ◽  
Author(s):  
Rolf W. Saalfrank ◽  
Roland Harbig ◽  
Oliver Struck ◽  
Frank Hampel ◽  
Eva Maria Peters ◽  
...  
Keyword(s):  
Coordination Polymer ◽  
Single Crystal ◽  
Coordination Polymers ◽  
Crystal Engineering ◽  
Coordination Compounds ◽  
Acetate Solution ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
X Ray ◽  
1D Coordination Polymer

Reaction of a methanolic copper(II) acetate solution with tetrazolyl enol derivatives 2a or 2b leads to the formation of the corresponding lD-coordination polymer 1∞[CuL2] 3a and pseudo 1D-coordination polymer [CuL2]2 3b, respectively. On the contrary, reaction of 2c with methanolic copper(II) acetate solution yields OH-bridged 1D-coordination polymer 1∞[CuL2(MeOH)2 3c. Single-crystal X-ray diffraction of the supramolecular species 3 established unequivocally the structures of the stairlike coordination compounds. Reaction of a methanolic copper(II) acetate solution with amidotetrazole derivative 6 leads to the formation of the lD-coordination polymer 1∞ [CuL2] 7. The structure of 7 has been established by X-ray structure analysis

Transition metal coordination complexes of chrysazin

CrystEngComm ◽  
2016 ◽  
Vol 18 (27) ◽  
pp. 5121-5129 ◽  
Author(s):  
Patrick J. Beldon ◽  
Sebastian Henke ◽  
Bartomeu Monserrat ◽  
Satoshi Tominaka ◽  
Norbert Stock ◽  
...  
Keyword(s):  
Transition Metal ◽  
Transition Metals ◽  
Single Crystal ◽  
Coordination Compounds ◽  
Coordination Complexes ◽  
Metal Coordination ◽  
X Ray Diffraction ◽  
X Ray

Eleven novel coordination compounds, composed of chrysazin (1,8-dihydroxyanthraquinone) and different first-row transition metals (Fe, Co, Ni, Cu), were synthesised and the structures determined by single-crystal X-ray diffraction.

scholarly journals Formation of Unsymmetrical Trinuclear Metallamacrocycles Based on Two Different Cone Calix[4]arene Macrocyclic Rings

Crystals ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 364 ◽  
Author(s):  
Mariia V. Kniazeva ◽  
Alexander S. Ovsyannikov ◽  
Daut R. Islamov ◽  
Aida I. Samigullina ◽  
Aidar T. Gubaidullin ◽  
...  
Keyword(s):  
Single Crystal ◽  
Coordination Compounds ◽  
Metallic Cluster ◽  
X Ray Diffraction ◽  
X Ray ◽  
Recognition Pattern ◽  
Carboxylate Groups ◽  
Different Types ◽  
Solvent Molecules ◽  
Oxygen Atoms

A combination of tetrasulfonylcalix[4]arene (3-4H) together with a calix[4]arene dicarboxylate derivative 2-4H led, in the presence of MII(NO3)2 (M = Co, Ni, Zn), to the formation of three novel isostructural metallomacrocycles of formula [M3(DMF)2(μ3-H2O)-(2-2H)-3]. The structure of the prepared coordination compounds was studied in the solid state using single crystal/powder X-ray diffraction studies. The X-ray diffraction on single crystal revealed that the structure of the obtained supramolecular complexes is composed of a trinuclear metallic cluster [M3]+6 held between one di-deprotonated molecule of (2-2H)2− offering two carboxylate groups for binding metal cations and one tetra-deprotonated compound 34−, where four oxygen atoms, belonging to four deprotonated phenolic moieties and three oxygen atoms coming from three SO2 groups, are coordinated with the cluster core. Thus, an example of an easily reproducible molecular recognition pattern involving two different types of calix[4]arene based ligands, displaying different coordination moieties, and trinuclear metallic clusters, is reported here. In addition, it has been shown that the cone moieties of the calixarene also encapsulate solvent molecules.

Synthesis, structures, and properties of Mn(II) and Cd(II) thiocyanato coordination compounds with 2,5-dimethylpyrazine as co-ligand

2016 ◽  
Vol 71 (5) ◽  
pp. 381-390 ◽  
Author(s):  
Stefan Suckert ◽  
Susanne Wöhlert ◽  
Christian Näther
Keyword(s):  
Liquid Phase ◽  
Single Crystal ◽  
Powder Diffraction ◽  
Coordination Compounds ◽  
Water Molecules ◽  
X Ray Diffraction ◽  
X Ray ◽  
Structures And Properties ◽  
Distorted Octahedra ◽  
Pure Phases

AbstractReaction of manganese (II) thiocyanate with 2,5-dimethylpyrazine leads to the formation of three new coordination compounds of compositions Mn(NCS)2(2,5-dimethylpyrazine)2(H2O)2 (1), Mn(NCS)2(H2O)2(MeOH)2-tris(2,5-dimethylpyrazine) solvate (2), and Mn(NCS)2 (H2O)4-tetrakis(2,5-dimethylpyrazine) solvate (3) that were characterized by single crystal X-ray diffraction. In their crystal structures, the Mn(II) cations are sixfold coordinated by two terminally N-bonded thiocyanato anions and two water molecules as well as by two 2,5-dimethylpyrazine ligands (1), two ethanol (2), or two water molecules (3), within slightly distorted octahedra. In compounds 2 and 3, additional 2,5-dimethylpyrazine ligands are located in the cavities of the structures as solvate molecules. X-ray powder diffraction has shown that compounds 1 and 2 cannot be prepared as pure phases and that batches of compound 3 contain only minor traces of a contamination. Differential thermoanalysis and thermogravimetry have revealed that upon heating of compound 3, an intermediate of composition Mn(NCS)2(2,5-dimethylpyrazine) (4) is formed, which cannot be obtained from solution. To mimic the structure of 4, single crystals of a Cd compound of the same composition (5) were prepared from the liquid phase, and single crystal X-ray analysis has shown that it is isotypic to 4.

Synthesis and characterization of ITr-protected group 11 metal trimethylsilylchalcogenolates

2020 ◽  
pp. 1-9
Author(s):  
Dickron R. Nahhas ◽  
John F. Corrigan
Keyword(s):  
Single Crystal ◽  
Diffraction Analysis ◽  
Coordination Compounds ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Protected Group ◽  
Copper Coordination

This work describes the synthesis of group 11 metal trimethylsilylchalcogenolate complexes [(ITr)M-ESiMe3] stabilized by the large NHC ligand bis-1,3-tritylimidazole-2-ylidene (ITr). The thiolates and selenolates of Cu, Ag, and Au are accessed from either [(ITr)MOAc] (M = Cu, Ag) and E(SiMe3)2 or [(ITr)AuCl] and Li[ESiMe3] (E = S, Se). All complexes were characterized spectroscopically and, for the copper coordination compounds, via single crystal X-ray diffraction analysis.

The silver(I) complex [HB{3-(CF3),5-(CH3)Pz}3]AgNCCH3supported by a partially fluorinated scorpionate ligand

2016 ◽  
Vol 72 (11) ◽  
pp. 853-856 ◽  
Author(s):  
H. V. Rasika Dias ◽  
Naveen Kulkarni
Keyword(s):  
Coordination Chemistry ◽  
Single Crystal ◽  
Diffraction Analysis ◽  
Electronic Properties ◽  
Coordination Sphere ◽  
Metal Coordination ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scorpionate Ligand

Tris(pyrazolyl)borates are used extensively in metal coordination chemistry and belong to a class of ligands generally referred to as scorpionates. The steric and electronic properties of these ligands can be modified quite easily by varying the substituents on the 3-, 4-, and 5-positions of the pyrazolyl moieties on the B atom. Fluorinated tris(pyrazolyl)borates are useful in the stabilization of rare silver(I) complexes. The silver(I) adduct (acetonitrile-κN){tris[5-methyl-3-(trifluoromethyl)pyrazol-1-yl-κN2]hydroborato}silver(I), [Ag(C15H13BF9N6)(CH3CN)] or [HB{3-(CF3),5-(CH3)Pz}3]AgNCCH3, was obtained by treating [HB{3-(CF3),5-(CH3)Pz}3]Na with CF3SO3Ag in the presence of acetonitrile, and was isolated in 85% yield. Single-crystal X-ray diffraction analysis reveals that the AgIcenter has a pseudo-tetrahedral all-nitrogen coordination sphere, and is supported by a tris(pyrazolyl)borate ligand that binds to the AgIcenter in a κ3-fashion.

Gold(I)-Komplexe sekundärer Phosphine / Gold(I) Complexes of Secondary Phosphines

1989 ◽  
Vol 44 (12) ◽  
pp. 1503-1508 ◽  
Author(s):  
Hubert Schmidbaur ◽  
Gabriele Weidenhiller ◽  
Aref A. M. Aly ◽  
Oliver Steigelmann ◽  
Gerhard Müller
Keyword(s):  
Single Crystal ◽  
Coordination Compounds ◽  
Good Yield ◽  
Steric Effects ◽  
Monoclinic Space Group ◽  
X Ray Diffraction ◽  
Data Set ◽  
X Ray ◽  
Intermolecular Contacts ◽  
Secondary Phosphines

Gold(I) complexes with secondary phosphines R2PH (la—d) of the type R2PH · AuCl (2a—d) have been obtained in good yield from reactions of (carbonyl)chlorogold(I) and the corresponding ligand in diethylether. Both compounds 2a, b bearing aromatic substituents with R = 2,4,6-trimethylphenyl (mesityl) and 2-methylphenyl (o-tolyl), and compounds 2c, d with the bulky alkyl substituents R = t-butyl and R = cyclohexyl, resp., are air-stable crystalline solids. — The coordination compounds have been characterized by NMR and IR data, and — in the cases of 2b and 2c — by single crystal X-ray diffraction studies. Crystals of these two compounds are both monoclinic, space group P21/c with four formula units (Z = 4). The analysis shows independent monomers for compound 2c with no intermolecular Au···Au contacts. Molecules of 2b are arranged in centrosymmetrical dimers (head to tail) with an Au···Au distance of 3.56 Å and a dihedral angle P—Au—Au′—P′ of 180°. (This structural study is as yet incomplete and suffers from an unsatisfactory data set for 2b.) It appears that intermolecular contacts are largely controlled by steric effects.

scholarly journals Aspherical-Atom Modeling of Coordination Compounds by Single-Crystal X-ray Diffraction Allows the Correct Metal Atom To Be Identified

ChemPhysChem ◽  
2014 ◽  
Vol 16 (2) ◽  
pp. 412-419 ◽  
Author(s):  
Birger Dittrich ◽  
Claudia M. Wandtke ◽  
Alke Meents ◽  
Kevin Pröpper ◽  
Kartik Chandra Mondal ◽  
...  
Keyword(s):  
Single Crystal ◽  
Metal Atom ◽  
Coordination Compounds ◽  
X Ray Diffraction ◽  
X Ray

Two CoII Compounds Showing Interesting Magnetic Properties Modulated by Supramolecular Interactions

2015 ◽  
Vol 68 (3) ◽  
pp. 433
Author(s):  
Xiao-Min Zhang ◽  
Li-Na Meng ◽  
Jian-Qiang Li ◽  
Xue-Feng Feng ◽  
Ming-Biao Luo ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Magnetic Susceptibility ◽  
Single Crystal ◽  
Direct Current ◽  
Coordination Compounds ◽  
Tricarboxylic Acid ◽  
Magnetic Susceptibility Measurement ◽  
Supramolecular Interactions ◽  
X Ray Diffraction ◽  
X Ray

Two new CoII coordination compounds, namely Co[(cis-trans)-L](nip)·H2O (1) and Co[(cis-cis)-L](Hbtc)·2H2O (2) (L = N1,N4-di(pyridin-3-yl)terephthalamide, H2nip = 5-nitroisophthalic acid, H3btc = benzene-1,3,5-tricarboxylic acid), were synthesised hydrothermally and characterised by single crystal X-ray diffraction and direct current magnetic susceptibility measurement. Interestingly, the results disclose somewhat tuneable magnetic properties for compounds 1 and 2, mainly due to the distinct supramolecular interactions.

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