scholarly journals Crystal structure of bis(N,N′-dimethylthiourea-κS)bis(thiocyanato-κN)cobalt(II)

2020 ◽  
Vol 76 (9) ◽  
pp. 1476-1481
Author(s):  
Aleksej Jochim ◽  
Rastko Radulovic ◽  
Inke Jess ◽  
Christian Näther

During systematic investigations on the synthesis of coordination polymers with Co(NCS)2 involving different thiourea derivatives as coligands, crystals of the title compound Co(NCS)2(N,N′-dimethylthiourea)2, or [Co(C3H8N2S)2(NCS)2], were obtained. These crystals were non-merohedric twins and therefore, a twin refinement using data in HKLF-5 format was performed. In the crystal structure of this compound, the CoII cations are coordinated by two N-terminally bonded thiocyanate anions as well as two S-bonding N,N′-dimethylthiourea molecules, forming two crystallographically independent discrete complexes each with a strongly distorted tetrahedral geometry. An intricate network of intermolecular N—H...S and C—H...S hydrogen bonds can be found between the complexes. The thermogravimetric curve of the title compound shows two discrete steps in which all coligand molecules have been emitted, which is also accompanied by partial decomposition of the cobalt thiocyanate. If the measurement is stopped after the first mass loss, only broad reflections of CoS can be found in the XRPD pattern of the residue, which proves that this compound decomposes completely upon heating. However, at lower temperatures an endothermic signal can be found in the DTA and DSC curve, which corresponds to melting, as proven by thermomicroscopy.

2012 ◽  
Vol 68 (8) ◽  
pp. m1099-m1099 ◽  
Author(s):  
Azadeh Tadjarodi ◽  
Keyvan Bijanzad ◽  
Behrouz Notash

In the title compound, [HgCl2(C6H8N2)2], the two independent HgIIcations are each located on a twofold rotation axis and coordinated by two pyridine N atoms from two 2-amino-3-methylpyridine ligands and two Cl−anions in a distorted tetrahedral geometry. An intramolecular N—H...Cl hydrogen bond occurs in each independent complex molecule. Intermolecular N—H...Cl hydrogen bonds occur in the crystal structure.


2015 ◽  
Vol 71 (5) ◽  
pp. m110-m111 ◽  
Author(s):  
Gerhard Laus ◽  
Volker Kahlenberg ◽  
Herwig Schottenberger

The title compound, (C10H21N3)[CuCl4], is composed of one 1-[2-(diethylazaniumyl)ethyl]-3-methylimidazolium dication and a tetrachloridocuprate(II) dianion. The anion adopts a distorted tetrahedral geometry. Bifurcated interionic N—H...Cl hydrogen bonds and several C—H...Cl contacts are observed, leading to a layer-like arrangement of the components parallel to (100).


2006 ◽  
Vol 62 (7) ◽  
pp. m1719-m1721 ◽  
Author(s):  
Luiz Everson da Silva ◽  
Antonio Carlos Joussef ◽  
Sabine Foro ◽  
Boris Schmidt

In the title compound, [Zn(C15H10FN2O2 S)2]·0.5H2O, the Zn atom has a distorted tetrahedral geometry, formed by the N atoms of the quinoline and the sulfonamide groups. The water molecule occupies a special position on a twofold axis. Intermolecular C—H...O hydrogen bonds to the sulfonyl O atoms link the molecules into a three-dimensional network.


2012 ◽  
Vol 68 (8) ◽  
pp. o2573-o2573 ◽  
Author(s):  
Muhammad Nadeem Arshad ◽  
Muhammad Danish ◽  
Muhammad Nawaz Tahir ◽  
Savera Khalid ◽  
Abdullah M. Asiri

In the title compound, C12H16N2O6S, the S atom adopts a distorted tetrahedral geometry with an O—S—O angle of 119.76 (13)°. The nitro group is twisted by 35.34 (2)° with respect to the aromatic ring; it accepts an N—H...O hydrogen bond, resulting in aS(7) motif. In the crystal, N—H...O and O—H...O hydrogen bonds connect the molecules into an infinite chain along theaaxis. The methyl C atoms of the isopropyl group are disordered in a 1:1 ratio.


2012 ◽  
Vol 68 (4) ◽  
pp. m496-m497 ◽  
Author(s):  
Wojciech Starosta ◽  
Janusz Leciejewicz

The structure of the title compound, {(N2H5)[Li3(C6H2N2O4)2(H2O)2]·H2O}n, is composed of molecular dimers, each built up of two symmetry-related LiIions with distorted trigonal–bipyramidal coordinations bridged by two deprotonated ligand moleculesviatheirN,O-bonding sites. Doubly solvated LiIions with a distorted tetrahedral geometry link adjacent dimers, forming a polymer generated by bridging bidentate carboxylato O atoms to LiIions in adjacent dimers, forming anionic layers parallel to theacplane with monoprotonated hydrazinium cations and crystal water molecules positioned between them. The layers are held together by an extended system of hydrogen bonds in which the hydrazinium cations and coordinated and crystal water molecules act as donors and carboxylate O atoms act as acceptors.


2012 ◽  
Vol 68 (6) ◽  
pp. m826-m826
Author(s):  
Hong Chen ◽  
Heng Xu

In the two-dimensional title coordination polymer, [Zn(C8H4O4)(C14H14N4)] n , the ZnII atom adopts a distorted tetrahedral geometry, being ligated by two O atoms from two different benzene-1,3-dicarboxylate dianions and two N atoms from two symmetry-related 1,2-bis(imidazol-1-ylmethyl)benzene molecules. The dihedral angles between the imidazole rings and the benzene ring in the neutral ligand are 76.31 (13) and 85.33 (15)°. The ZnII atoms are bridged by dicarboxylate ligands, forming chains parallel to the a axis, which are further linked by 1,2-bis(imidazol-1-ylmethyl)benzene molecules, generating a two-dimensional layer structure parallel to the ac plane. The crystal structure is enforced by intralayer and interlayer C—H...O hydrogen bonds.


2007 ◽  
Vol 63 (3) ◽  
pp. m654-m655 ◽  
Author(s):  
Yi-Jun Wei ◽  
Feng-Wu Wang ◽  
Qi-Yong Zhu

The title compound, [ZnBr2(C13H19ClN2O)], is a mononuclear Schiff base zinc(II) complex. The Zn atom in the compound is four-coordinated by one imine N and one phenolate O atom of the Schiff base ligand and by two terminal bromide anions in a tetrahedral geometry. In the crystal structure, molecules are linked through intermolecular N—H...O and C—H...Br hydrogen bonds, forming layers parallel to the bc plane.


IUCrData ◽  
2018 ◽  
Vol 3 (8) ◽  
Author(s):  
Niloufar Khojandi ◽  
Nigam P. Rath ◽  
Myron W. Jones

In the title compound, C20H20NOP, the P atom, with a distorted tetrahedral geometry, is attached to an O atom, two phenyl groups, and a 3,5-dimethylaniline group. The N—P—C [102.29 (12) and 108.97 (12)°] and C—P—C [107.14 (12)°] bond angles are all smaller than the ideal 109.5° tetrahedral bond angle, whereas the O—P—C [113.07 (12) and 110.62 (12)°] and O—P—N [114.24 (13)°] angles are all larger than 109.5°. A weak intramolecular C—H...O hydrogen bond helps to establish the molecular conformation. In the crystal, the molecules are linked by N—H...O hydrogen bonds, generating [001] chains.


2012 ◽  
Vol 68 (6) ◽  
pp. o1813-o1813 ◽  
Author(s):  
Akbar Raissi Shabari ◽  
Mehrdad Pourayoubi ◽  
Hassan Fadaei ◽  
Marek Nečas ◽  
Michal Babiak

The P atom in the title compound, C16H17Cl3N3O2P, is bonded in a distorted tetrahedral geometry with the phosphoryl and carbonyl groups anti with respect to one another. In the crystal, molecules are linked through (N—H)2...O(=P) and N—H...O(=C) hydrogen bonds into chains along [001]. The phosphoryl O atom acts as a double hydrogen-bond acceptor.


Author(s):  
Perdita Arndt ◽  
Kathleen Schubert ◽  
Vladimir V. Burlakov ◽  
Anke Spannenberg ◽  
Uwe Rosenthal

The crystal structure of the title compound, [Hf(C10H15)2(C4H9)2], reveals two independent molecules in the asymmetric unit. The diffraction experiment was performed with a racemically twinned crystal showing a 0.529 (5):0.471 (5) component ratio. Each HfIVatom is coordinated by two pentamethylcyclopentadienyl and twon-butyl ligands in a distorted tetrahedral geometry, with the cyclopentadienyl rings inclined to one another by 45.11 (15) and 45.37 (16)°. In contrast to the isostructural di(n-butyl)bis(η5-pentamethylcyclopentadienyl)zirconium(IV) complex with a noticeable difference in the Zr–butyl bonding, the Hf—Cbutylbond lengths differ from each other by no more than 0.039 (3) Å.


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