Bis[2-(dimethylamino)ethanol-κ2 N,O](2,4-pentanedionato-κ2 O,O′)nickel(II) acetate

2006 ◽  
Vol 62 (4) ◽  
pp. m824-m826
Author(s):  
Sultan Muhammad ◽  
Muhammad Mazhar ◽  
Matthias Zeller ◽  
Allen D. Hunter

The Ni atom in the title complex, [Ni(C5H7O2)(C4H11NO)2](C2H3O2), has distorted octahedral coordination. The O atoms of the acetate ion are hydrogen bonded to the OH groups of the 2-(dimethylamino)ethanol ligands.

2007 ◽  
Vol 63 (3) ◽  
pp. m845-m846 ◽  
Author(s):  
Ying-Ju Fan ◽  
Le Wang ◽  
Jian-Ping Ma ◽  
Zhong-Xi Sun

Reaction of indium(III) chloride with (E)-1-[1-(2-pyridyl)ethylidene]thiosemicarbazide afforded the title complex, [In(C8H9N4S)Cl2(C2H5OH)]. The ligand is in the enol form coordinating to the InIII atom through one S atom and two N atoms. The InIII atom is further coordinated by two Cl atoms and an ethanol molecule to complete a distorted octahedral coordination geometry.


2012 ◽  
Vol 68 (6) ◽  
pp. m857-m857 ◽  
Author(s):  
Chao-Hu Xiao ◽  
Xue-Yan Song ◽  
Zan Sun ◽  
Ping Cao ◽  
Ting Pang

The central CoII ion in the title complex, [Co(C16H19N5)2](NO3)2, is located on a twofold rotation axis and has a slightly distorted octahedral coordination sphere. It is bonded to six N atoms from two 2-[bis(3,5-dimethyl-1H-pyrazol-1-yl)methyl]pyridine ligands. In the crystal, molecules are linked by weak C—H...O interactions.


2006 ◽  
Vol 62 (5) ◽  
pp. m1079-m1080
Author(s):  
E Yang ◽  
Yi Zheng ◽  
Gu-Yong Chen

In the title complex, [Cu(C8H4O4)(C10H9N3)] n , the benzene-1,4-dicarboxylate dianions bridge the CuII atoms to form polymeric complex chains. The CuII atom has a distorted octahedral coordination geometry. The centroid-to-centroid separation of 3.932 (2) Å indicates π–π stacking between nearly parallel pyridine rings.


2014 ◽  
Vol 70 (12) ◽  
pp. 483-485
Author(s):  
Olgerd O. Shtokvish ◽  
Lyudmila I. Koval ◽  
Vasyl I. Pekhnyo

The title complex, systematic name hexakis(μ2-4-tert-butoxy-4-oxobut-2-en-2-olato)-1:2κ9O2,O4:O2;2:3κ9O2,O4:O2-trizinc, [Zn3(C8H13O3)6], synthesized fromtert-butyl acetoacetate and diethylzinc, consists of trinuclear centrosymmetric molecules of an approximateC3isymmetry. The three metal cations are arranged in a linear fashion, with the central ZnIIatom located on a centre of symmetry. All three metal cations exhibit a distorted octahedral coordination geometry. The terminal ZnIIcations are chelated by threetert-butyl acetoacetate ligands and these units are connected to the central ZnIIatom by the bridging enolate O atoms.


2007 ◽  
Vol 63 (11) ◽  
pp. m2654-m2654 ◽  
Author(s):  
Chun-Bao Tang

The title complex, [Ni(C12H17N2O2)2], possesses a crystallographically imposed center of symmetry occupied by the NiII ion. Each 2-methoxy-6-[3-(methylamino)propyliminomethyl]phenolate ligand coordinates the Ni atom in a tridentate mode [Ni—O = 2.0356 (18) Å, and Ni—N = 2.048 (2) and 2.184 (2) Å], resulting in a distorted octahedral coordination geometry.


2006 ◽  
Vol 62 (7) ◽  
pp. m1506-m1507 ◽  
Author(s):  
Huan-Ran Xing ◽  
Xin-Hua Li

In the polymeric title complex, [Co(TBC)(BPE)(H2O)2] n [TBC is the 2,5-dicarboxybenzene-1,4-dicarboxylate dianion (C10H4O8) and BPE is 1,2-bis(4-pyridyl)ethene (C12H10N2)], the CoII ion, located on an inversion centre, assumes a distorted octahedral coordination geometry. The TBC and BPE ligands are located across individual inversion centres and bridge neighbouring CoII ions to form two-dimensional polymeric sheets.


2013 ◽  
Vol 69 (2) ◽  
pp. m105-m105 ◽  
Author(s):  
Xiu-Li Wu ◽  
Ru-Fei Ye ◽  
Ai-Quan Jia ◽  
Qun Chen ◽  
Qian-Feng Zhang

The title complex, [RuBr2(C5H5N)4], contains two independent complex molecules in each of which the RuIIatom is located on a site of 222 symmetry and has a distorted octahedral coordination geometry with four pyridine N atoms and two Br atoms. The Br aroms aretrans-disposed as a result of symmetry.


IUCrData ◽  
2016 ◽  
Vol 1 (9) ◽  
Author(s):  
Qiuwen Wang ◽  
Yihan Xiong ◽  
Xuebin Deng

Reaction of the Schiff base ligand (R)-2-(pyrrol-2-ylmethyleneamino)-2′-methoxy-6,6′-dimethyl-1,1′-biphenyl with tetrakis(dimethylamido)vanadium in toluene gives the mononuclear VIVtitle complex, [V(C2H6N)2(C20H19N2O)2]·C7H8, which was isolated as red crystals. The VIVcation is coordinated by two monoanionic bidentate Schiff base ligands and two N atoms of two dimethylamide anions in a VN6distorted octahedral coordination geometry, in which two N atoms from the dimethylamide anions are placed in acis-configuration.


2007 ◽  
Vol 63 (3) ◽  
pp. m737-m739 ◽  
Author(s):  
Wen-Dong Song ◽  
Xian-Xia Guo ◽  
Guo Rong-Fa

In the title complex, [Mn(C7H2N2O7)(C10H8N2)] n , the MnII atom has a distorted octahedral coordination geometry, defined by two N atoms from the 2,2′-bipyridine ligand and four O atoms from two 3,5-dinitrosalicylate dianions. One carboxylate O atom acts as a bridge between adjacent metal centres to form a one-dimensional chain. The Mn...Mn distance is 4.315 (6) Å. The crystal packing is stabilized by intermolecular C—H...O hydrogen interactions.


2007 ◽  
Vol 63 (11) ◽  
pp. m2729-m2729
Author(s):  
Jian Yu

The anion of the title complex, (C12H14N2)[Co2(C6H4O7)2(H2O)2], is a centrosymmetric edge-shared bioctahedral dimer, in which the two Co atoms are bridged by two alkoxide O atoms of the fully deprotonated citrate ligands. All of the carboxylate groups coordinate in a monodentate fashion to terminal positions, and two water molecules complete the slightly distorted octahedral coordination. The dinuclear cation complex and the dianion are organized around inversion centers. Supramolecular O—H...O and N—H...O interactions stabilize the architecture.


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