The title complex, [Cu(C(11)H(10)N(2)O(2))(2)](BF(4))(2)·2H(2)O, was isolated as a dihydrate from a 1:2 molar mixture of copper(II) tetra-fluoridoborate hexa-hydrate with di-2-pyridyl ketone in aqueous solution. The centrosymmetric complex cation is structurally similar to that found in previously reported salts and exhibits Cu-O bonds deviating by 25 degrees from an octa-hedral geometry by the so-called 'off-axis angle' distortion. The BF(4) (-) anion exhibits a two site disorder of the fluorine atoms [ratio 0.210 (8):0.790 (8)].
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http://dx.doi.org/10.1107/S1600536809016973 | DOI Listing |
IUCrdata
June 2023
Department of Inorganic Chemistry and Technology, Jožef Stefan Institute, Jamova 39 1000 Ljubljana, Slovenia.
The crystal structure of the low-temperature modification of Ba(BF)(HO), barium bis(tetra-fluorido-borate) trihydrate, was determined at 150 K. In contrast to the room-temperature modification, which crystallizes in the space group 222 [ = 7.1763 (6), = 18.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
June 2022
Department of Chemistry, Keene State College, Keene NH 03435-2001, USA.
The reaction of [Cu(CHCN)](BF) with 1-methyl-1,3-imidazolidine-2-thione {SCH(NMe)NH}, under aerobic conditions at room temperature, yielded an unusual one-dimensional coordination polymer, namely, -poly[[[(1-meth-yl-1,3-imidazolidine-2-thione-κ)copper(I)]-μ-(1-methyl-1,3-imidazolidine-2-thione)-κ :-copper(I)-μ-[3,3'-(sulfanedi-yl)bis-(1-methyl-1,3-imidazolidine-2-thione)]-κ ,','':,''] bis-(tetra-fluorido-borate)], {[Cu(CHNS)(CHNS)](BF)} or [Cu(κ: -N-S-N- )(κ: -NH)(κ: -NH)] (BF) [ = SC H(NMe)NH] with sulfur-bridged {Cu S} central cores. The generated bis-(1-methyl-1,3-imidazolidinyl-2-thione) sulfide [{SCH(NMe)NSN(NMe)CHS; abbrev. -N-S-N- ] ligand, in combin-ation with 1-methyl-1,3-imidazolidine-2-thione ( -NH) ligands, construct this coordination polymer.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
May 2018
Austin College, 900 N Grand, Sherman, TX 75090-4400, USA.
The crystal structure of a platinum(II) supra-molecular building block, [Pt(dbbpy)(NCCH)](BF) (dbbpy = 4,4'-di--butyl-2,2'-bi-pyridine, CHN) is an example of a rare head-to-head dimer, even with the bulky -butyl groups of the bi-pyridine. This packing motif still enables significant π-π inter-actions between two pyridyl groups, and may result from the close proximity of the tetra-fluorido-borate ions to the platinum(II) complexes, resulting in intra-molecular H⋯F distances between 2.156 and 2.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
April 2017
Institute of Materials, China Academy of Engineering Physics, Jiangyou 621908, People's Republic of China.
The mononuclear copper title complex {,,','-tetra-kis-[(6-methyl-pyridin-2-yl)meth-yl]ethane-1,2-di-amine-κ}copper(II) bis-(tetra-fluorido-borate), [Cu(CHN)](BF), is conveniently prepared from the reaction of Cu(BF)·6HO with ,,','-tetra-kis-[(6-methyl-pyridin-2-yl)meth-yl]ethane-1,2-di-amine (tmpen) in aceto-nitrile at room temperature in air. The complex shows a distorted octa-hedral environment around the Cu cation (site symmetry 2) and adopts the centrosymmetric space group 2/. The presence of the 6-methyl substituent hinders the approach of the pyridine group to the Cu core.
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June 2015
Daegu Gyeongbuk Institue of Science & Technology (DGIST), Daegu 711-873, Republic of Korea.
In the structure of the title salt, [Co(C6H6N2)2(H2O)2](BF4)2, the Co(II) atom is located on an inversion centre. The transition metal is in a slightly distorted octa-hedral coordination environment, defined by the cyano N atoms of four hex-3-enedi-nitrile ligands in equatorial positions and the O atoms of two water mol-ecules in axial positions. The bridging mode of the hex-3-enedi-nitrile ligands leads to the formation of cationic chains extending parallel to [1-10].
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