The asymmetric unit of the title compound, {[Co(CHO)(HO)]·2CHNO} or {[Co(Hdondc)(HO)]·2DMF} , comprises half of a Co ion, half of a 1,5-di-hydroxy-naphthalene-2,6-di-carboxyl-ate dianion (Hdondc), two water mol-ecules and a di-methyl-formamide (DMF) mol-ecule. The Co ion, which is located on a crystallographic inversion center, exhibits a distorted six-coord-inated octa-hedral geometry with two oxygen atoms of the Hdondc ligand and four oxygen atoms of the water mol-ecules. The carboxyl-ate group is almost coplanar with the naphthalene moiety and shows monodentate coordination to the Co ion. The Co ions are bridged by the Hdondc ligand to form a one-dimensional chain. The hy-droxy groups of the ligand have intra-chain hydrogen bonding inter-actions with coordinated water mol-ecules. The coordinated water mol-ecules exhibit not only intra-chain hydrogen bonding inter-actions, but also inter-chain hydrogen-bonding inter-actions. The chains are connected by inter-chain hydrogen-bonding inter-actions and are arranged in parallel to form a two-dimensional network. The chains are further connected by inter-chain hydrogen-bonding inter-actions the DMF mol-ecules and C-H⋯π inter-actions to give a three-dimensional network.
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http://dx.doi.org/10.1107/S2056989025000982 | DOI Listing |
Acta Crystallogr E Crystallogr Commun
March 2025
Toyota Central R&D Labs., Inc., 41-1 Yokomichi, Nagakute, Aichi 480-1192, Japan.
The asymmetric unit of the title compound, {[Co(CHO)(HO)]·2CHNO} or {[Co(Hdondc)(HO)]·2DMF} , comprises half of a Co ion, half of a 1,5-di-hydroxy-naphthalene-2,6-di-carboxyl-ate dianion (Hdondc), two water mol-ecules and a di-methyl-formamide (DMF) mol-ecule. The Co ion, which is located on a crystallographic inversion center, exhibits a distorted six-coord-inated octa-hedral geometry with two oxygen atoms of the Hdondc ligand and four oxygen atoms of the water mol-ecules. The carboxyl-ate group is almost coplanar with the naphthalene moiety and shows monodentate coordination to the Co ion.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
March 2025
A new cobalt complex, bis-[tris-(amino-thio-urea)cobalt(III)] bis-[2-(carb-oxy-methyl)-2-hy-droxy-butane-dioato]cobalt(II) tetra-nitrate tetra-hydrate, [Co(CHNS)][Co(CHO)](NO)·2HO, designated as [Co(tsc)][Co(cit)](NO)·4HO, was synthesized. Two crystallographically independent cobalt centers are present. In the first, the central metal atom is chelated by three thio-semicarbazide ligands in a bidentate fashion whereas the second, positioned on a crystallographic inversion center, is hexa-coordinated by two citrate anions in a distorted octa-hedral geometry.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
February 2025
Institute of Inorganic Chemistry, Kiel University, Max-Eyth-Str. 2, 24118 Kiel, Germany.
Single crystals of the title compound, [Ce(CHCOO)(SO)(HO)] , were obtained serendipitously by the reaction of Ce(NO)·6HO with 2,5-thio-phenedi-carb-oxy-lic acid (HTDC) and acetic acid in a mixture of ethanol and water, where it is assumed that the sulfate ions leached from the Teflon reactor, which was treated with per-oxy-monosulfuric acid prior to its use. Its asymmetric unit consists of one Ce cation, one sulfate dianion, one acetate anion and two crystallographically independent water mol-ecules, all of them located in general positions. The cerium cations are coordinated by three acetate anions (one ,-chelating) and three sulfate dianions that are related by symmetry as well as two independent water mol-ecules within an irregular CeO coordination geometry.
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February 2025
Department of Biochemistry Chemistry and Physics Georgia Southern University, Armstrong Campus 11935 Abercorn Street Savannah GA 31419 USA.
The reaction of one equivalent of zinc(II) halide salts with two equivalents of iso-quinoline -oxide (iQNO; CHNO) in methanol yields compounds of the general formula [Zn (iQNO)], with = Cl (), Br () and I (). However, starting with zinc(II) perchlorate or nitrate leads to the formation of complex ions with the compositions [Zn(iQNO)]() for = ClO (), and [Zn(iQNO)(HO)](iQNO) for = NO (). Complexes (), () and (), namely di-chlorido-bis-(iso-quinoline -oxide-κ)zinc(II) [ZnCl(CHNO)], di-bromido-bis-(iso-quinoline -oxide-κ)zinc(II) [ZnBr(CHNO)], and di-iodido-bis-(iso-quinoline -oxide-κ)zinc(II) [ZnI(CHNO)], each exhibit a distorted tetra-hedral coordination geometry around the zinc(II) ion coordinated by two iQNO ligands bound through the oxygen atom and two halide ions.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
February 2025
L. V. Pisarzhevskii Institute of Physical Chemistry of the National Academy of Sciences of Ukraine, Prospekt Nauki 31, 03028, Kyiv, Ukraine.
The asymmetric units of -poly[[(1,4,8,11-tetra-aza-cyclo-tetra-decane-κ , , , )nickel(II)]-μ-sulfato-κ : ], [Ni(SO)(CHN)] (), and -poly[[(1,4,8,11-tetra-aza-cyclo-tetra-decane-κ , , , )nickel(II)]-μ-sul-fato-κ : ] hemi[4,4',4'',4'''-(2,2',4,4',6,6'-hexa-methyl-[1,1'-biphen-yl]-3,3',5,5'-tetra-yl)tetra-benzoic acid] nona-hydrate], {[Ni(SO)(CHN)]·CHO·18HO} (), consist of two crystallographically unique centrosymmetric macrocyclic dications and a sulfate dianion. In it includes additionally a mol-ecule of the undissociated acid (2,2',4,4',6,6'-hexa-meth-yl[1,1'-biphen-yl]-3,3',5,5'-tetra-yl)tetra-(benzoic acid) located on a crystallographic twofold axis and nine highly disordered water mol-ecules of crystallization. In both compounds, the metal ions are coordinated in the equatorial plane by the four secondary N atoms of the macrocyclic ligand, which adopts the most energetic-ally stable -III conformation.
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