A fixation mode of gold from solutions using heterogeneous reaction of cadmium dicyclohexyl dithiophosphate with H[AuCl4]. Structural and (13C, 31P) CP/MAS NMR studies and thermal behaviour of crystalline polymeric gold(I) dicyclohexyl dithiophosphate and bis(dicyclohexylthiophosphoryl) disulphide

► Doubly-bridged binuclear gold(I) di-cyclo-hexyldithiophosphate comprising aurophilic bonds. ► Supramolecular self-organisation of polymeric chains involving secondary bonds Au⋯S. ► Thermal decomposition of the complex successively yields [Au2(S2PO)2] and metallic Au. ► Centrosymmetric molecule of...

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Published inJournal of molecular structure Vol. 1034; pp. 152 - 161
Main Authors Ivanov, Alexander V., Korneeva, Eugenia V., Lutsenko, Irina A., Gerasimenko, Andrey V., Antzutkin, Oleg N., Larsson, Anna-Carin, Sergienko, Valentin I.
Format Journal Article
LanguageEnglish
Published Elsevier B.V 27.02.2013
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Abstract ► Doubly-bridged binuclear gold(I) di-cyclo-hexyldithiophosphate comprising aurophilic bonds. ► Supramolecular self-organisation of polymeric chains involving secondary bonds Au⋯S. ► Thermal decomposition of the complex successively yields [Au2(S2PO)2] and metallic Au. ► Centrosymmetric molecule of bis(O,O′-di-cyclo-hexylthiophosphoryl) disulphide. ► 13C and 31P CP/MAS NMR characteristics of di-cyclo-hexyldithiophosphate compounds. Two novel compounds: polynuclear catena-poly[bis(μ3-O,O′-di-cyclo-hexyldithiophosphato-S,S,S′)digold(I)] (AuAu) (1) and crystalline bis(O,O′-di-cyclo-hexylthiophosphoryl)disulphide, (cyclo-C6H11O)2P(S)SS(S)P(O-cyclo-C6H11)2 (2) were prepared using heterogeneous reaction between freshly precipitated binuclear cadmium(II) dithiophosphate (Dtph), [Cd2{S2P(O-cyclo-C6H11}4] and H[AuCl4] in 2M hydrochloric acid. The isolated compounds 1 and 2 (the fixation mode of gold from the solution and the oxidised form of Dtph groups, respectively) have been studied by means of single-crystal X-ray diffraction, 13C and 31P cross-polarisation/magic-angle-spinning (CP/MAS) NMR spectroscopy and simultaneous thermal analysis (STA). Centrosymmetric binuclear molecule of 1, [Au2{S2P(O-cyclo-C6H11)2}2] comprises a pair of μ-bridging di-cyclo-hexyl Dtph ligands, linking two neighbouring gold atoms, and displays additional intramolecular aurophilic bond Au⋯Au. At the supramolecular level of structural self-organisation of complex 1, infinite polymeric zigzag chains arise due to pairs of the secondary bonds Au···S between neighbouring binuclear molecules. Centrosymmetric molecule of 2 displays two O,O′-di-cyclo-hexythiophosphoryl fragments, which are connected by the chemical bond S(1)S(1)a, and a planar zigzag array [SPSSPS] passing through the central part of the molecule. To characterise additionally the Dtph groups in both compounds 1 and 2, chemical shift anisotropy (CSA) parameters (δaniso and η) were calculated from spinning sideband manifolds in experimental 31P MAS NMR spectra. The thermal behaviour of complex 1 was studied using simultaneous thermal analysis (a combination of TG and DSC) under an argon atmosphere. The thermal behaviour displays stepwise mass loss, comprising thermal decompositions of the organic and inorganic parts of 1 with gold(I) dithio-meta-phosphate and reduced metallic gold as the intermediate and the final products, respectively.
AbstractList Two novel compounds: polynuclear catena-poly[bis(μ₃-O,O′-di-cyclo-hexyldithiophosphato-S,S,S′)digold(I)] (AuAu) (1) and crystalline bis(O,O′-di-cyclo-hexylthiophosphoryl)disulphide, (cyclo-C₆H₁₁O)₂P(S)SS(S)P(O-cyclo-C₆H₁₁)₂ (2) were prepared using heterogeneous reaction between freshly precipitated binuclear cadmium(II) dithiophosphate (Dtph), [Cd₂{S₂P(O-cyclo-C₆H₁₁}₄] and H[AuCl₄] in 2M hydrochloric acid. The isolated compounds 1 and 2 (the fixation mode of gold from the solution and the oxidised form of Dtph groups, respectively) have been studied by means of single-crystal X-ray diffraction, ¹³C and ³¹P cross-polarisation/magic-angle-spinning (CP/MAS) NMR spectroscopy and simultaneous thermal analysis (STA). Centrosymmetric binuclear molecule of 1, [Au₂{S₂P(O-cyclo-C₆H₁₁)₂}₂] comprises a pair of μ-bridging di-cyclo-hexyl Dtph ligands, linking two neighbouring gold atoms, and displays additional intramolecular aurophilic bond Au⋯Au. At the supramolecular level of structural self-organisation of complex 1, infinite polymeric zigzag chains arise due to pairs of the secondary bonds Au···S between neighbouring binuclear molecules. Centrosymmetric molecule of 2 displays two O,O′-di-cyclo-hexythiophosphoryl fragments, which are connected by the chemical bond S(1)S(1)ᵃ, and a planar zigzag array [SPSSPS] passing through the central part of the molecule. To characterise additionally the Dtph groups in both compounds 1 and 2, chemical shift anisotropy (CSA) parameters (δₐₙᵢₛₒ and η) were calculated from spinning sideband manifolds in experimental ³¹P MAS NMR spectra. The thermal behaviour of complex 1 was studied using simultaneous thermal analysis (a combination of TG and DSC) under an argon atmosphere. The thermal behaviour displays stepwise mass loss, comprising thermal decompositions of the organic and inorganic parts of 1 with gold(I) dithio-meta-phosphate and reduced metallic gold as the intermediate and the final products, respectively.
Two novel compounds: polynuclear catena-poly[bis( mu 3-O,O'-di-cyclo-hexyldithiophosphato-S,S,S')digol d(I)] (AuAu) (1) and crystalline bis(O,O'-di-cyclo-hexylthiophosphoryl)disulphide, (cyclo-C6H11O)2P(S)SS(S)P(O-cyclo-C6H11)2 (2) were prepared using heterogeneous reaction between freshly precipitated binuclear cadmium(II) dithiophosphate (Dtph), [Cd2{S2P(O-cyclo-C6H11}4] and H[AuCl4] in 2 M hydrochloric acid. The isolated compounds 1 and 2 (the fixation mode of gold from the solution and the oxidised form of Dtph groups, respectively) have been studied by means of single-crystal X-ray diffraction, 13C and 31P cross-polarisation/magic-angle-spinning (CP/MAS) NMR spectroscopy and simultaneous thermal analysis (STA). Centrosymmetric binuclear molecule of 1, [Au2{S2P(O-cyclo-C6H11)2}2] comprises a pair of mu -bridging di-cyclo-hexyl Dtph ligands, linking two neighbouring gold atoms, and displays additional intramolecular aurophilic bond Au?Au. At the supramolecular level of structural self-organisation of complex 1, infinite polymeric zigzag chains arise due to pairs of the secondary bonds AuADTADTADTS between neighbouring binuclear molecules. Centrosymmetric molecule of 2 displays two O,O'-di-cyclo-hexythiophosphoryl fragments, which are connected by the chemical bond S(1)S(1)a, and a planar zigzag array [SPSSPS] passing through the central part of the molecule. To characterise additionally the Dtph groups in both compounds 1 and 2, chemical shift anisotropy (CSA) parameters ([d]aniso and ?) were calculated from spinning sideband manifolds in experimental 31P MAS NMR spectra. The thermal behaviour of complex 1 was studied using simultaneous thermal analysis (a combination of TG and DSC) under an argon atmosphere. The thermal behaviour displays stepwise mass loss, comprising thermal decompositions of the organic and inorganic parts of 1 with gold(I) dithio-meta-phosphate and reduced metallic gold as the intermediate and the final products, respectively.
► Doubly-bridged binuclear gold(I) di-cyclo-hexyldithiophosphate comprising aurophilic bonds. ► Supramolecular self-organisation of polymeric chains involving secondary bonds Au⋯S. ► Thermal decomposition of the complex successively yields [Au2(S2PO)2] and metallic Au. ► Centrosymmetric molecule of bis(O,O′-di-cyclo-hexylthiophosphoryl) disulphide. ► 13C and 31P CP/MAS NMR characteristics of di-cyclo-hexyldithiophosphate compounds. Two novel compounds: polynuclear catena-poly[bis(μ3-O,O′-di-cyclo-hexyldithiophosphato-S,S,S′)digold(I)] (AuAu) (1) and crystalline bis(O,O′-di-cyclo-hexylthiophosphoryl)disulphide, (cyclo-C6H11O)2P(S)SS(S)P(O-cyclo-C6H11)2 (2) were prepared using heterogeneous reaction between freshly precipitated binuclear cadmium(II) dithiophosphate (Dtph), [Cd2{S2P(O-cyclo-C6H11}4] and H[AuCl4] in 2M hydrochloric acid. The isolated compounds 1 and 2 (the fixation mode of gold from the solution and the oxidised form of Dtph groups, respectively) have been studied by means of single-crystal X-ray diffraction, 13C and 31P cross-polarisation/magic-angle-spinning (CP/MAS) NMR spectroscopy and simultaneous thermal analysis (STA). Centrosymmetric binuclear molecule of 1, [Au2{S2P(O-cyclo-C6H11)2}2] comprises a pair of μ-bridging di-cyclo-hexyl Dtph ligands, linking two neighbouring gold atoms, and displays additional intramolecular aurophilic bond Au⋯Au. At the supramolecular level of structural self-organisation of complex 1, infinite polymeric zigzag chains arise due to pairs of the secondary bonds Au···S between neighbouring binuclear molecules. Centrosymmetric molecule of 2 displays two O,O′-di-cyclo-hexythiophosphoryl fragments, which are connected by the chemical bond S(1)S(1)a, and a planar zigzag array [SPSSPS] passing through the central part of the molecule. To characterise additionally the Dtph groups in both compounds 1 and 2, chemical shift anisotropy (CSA) parameters (δaniso and η) were calculated from spinning sideband manifolds in experimental 31P MAS NMR spectra. The thermal behaviour of complex 1 was studied using simultaneous thermal analysis (a combination of TG and DSC) under an argon atmosphere. The thermal behaviour displays stepwise mass loss, comprising thermal decompositions of the organic and inorganic parts of 1 with gold(I) dithio-meta-phosphate and reduced metallic gold as the intermediate and the final products, respectively.
Two novel compounds: polynuclear catena-poly[bis(3-O,O’-di-cyclo-hexyldithiophosphato-S,S,S’)digold(I)] (Au–Au) (1) and crystalline bis(O,O’-di-cyclo-hexylthiophosphoryl)disulphide, (cyclo-C6H11O)2P(S)S–S(S)P(O-cyclo-C6H11) (2) were prepared using heterogeneous reaction between freshly precipitated binuclear cadmium(II) dithiophosphate (Dtph), [Cd2{S2P(O-cyclo-C6H11}4] and H[AuCl4] in 2 M hydrochloric acid. The isolated compounds 1 and 2 (the fixation mode of gold from the solution and the oxidised form of Dtph groups, respectively) have been studied by means of single-crystal X-ray diffraction, 13C and 31P cross-polarisation / magic-angle-spinning (CP/MAS) NMR spectroscopy and simultaneous thermal analysis (STA). Centrosymmetric binuclear molecule of 1, [Au2{S2P(O-cyclo-C6H11)2}2] comprises a pair of -bridging di-cyclo-hexyl Dtph ligands, linking two neighbouring gold atoms, and displays additional intramolecular aurophilic bond Au···Au. At the supramolecular level of structural self-organisation of complex 1, infinite polymeric zigzag chains arise due to pairs of the secondary bonds Au···S between neighbouring binuclear molecules. Centrosymmetric molecule of 2 displays two O,O-di-cyclo-hexythiophosphoryl fragments, which are connected by the chemical bond S(1)–S(1)a, and a planar zigzag array [S=P–S–S–P=S] passing through the central part of the molecule. To characterise additionally the Dtph groups in both compounds 1 and 2, chemical shift anisotropy (CSA) parameters (aniso and) were calculated from spinning sideband manifolds in experimental 31P MAS NMR spectra. The thermal behaviour of complex 1 was studied using simultaneous thermal analysis (a combination of TG and DSC) under an argon atmosphere. The thermal behaviour displays stepwise mass loss, comprising thermal decompositions of the organic and inorganic parts of 1 with gold(I) dithio-meta-phosphate and reduced metallic gold as the intermediate and the final products, respectively.
Author Lutsenko, Irina A.
Ivanov, Alexander V.
Antzutkin, Oleg N.
Sergienko, Valentin I.
Gerasimenko, Andrey V.
Korneeva, Eugenia V.
Larsson, Anna-Carin
Author_xml – sequence: 1
  givenname: Alexander V.
  surname: Ivanov
  fullname: Ivanov, Alexander V.
  email: alexander.v.ivanov@chemist.com
  organization: Institute of Geology and Nature Management, Far Eastern Branch of the Russian Academy of Sciences, 675000 Blagoveschensk, Amur Region, Russia
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  givenname: Eugenia V.
  surname: Korneeva
  fullname: Korneeva, Eugenia V.
  organization: Institute of Geology and Nature Management, Far Eastern Branch of the Russian Academy of Sciences, 675000 Blagoveschensk, Amur Region, Russia
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  givenname: Irina A.
  surname: Lutsenko
  fullname: Lutsenko, Irina A.
  organization: Institute of Geology and Nature Management, Far Eastern Branch of the Russian Academy of Sciences, 675000 Blagoveschensk, Amur Region, Russia
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  givenname: Andrey V.
  surname: Gerasimenko
  fullname: Gerasimenko, Andrey V.
  organization: Institute of Chemistry, Far Eastern Branch of the Russian Academy of Sciences, 690022 Vladivostok, Russia
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  givenname: Oleg N.
  surname: Antzutkin
  fullname: Antzutkin, Oleg N.
  organization: Department of Physics, Warwick University, Coventry CV47AL, UK
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  givenname: Anna-Carin
  surname: Larsson
  fullname: Larsson, Anna-Carin
  organization: Chemistry of Interfaces, Luleå University of Technology, S-97187 Luleå, Sweden
– sequence: 7
  givenname: Valentin I.
  surname: Sergienko
  fullname: Sergienko, Valentin I.
  organization: Institute of Chemistry, Far Eastern Branch of the Russian Academy of Sciences, 690022 Vladivostok, Russia
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Keywords Aurophilic bonding
Bis(O,O′-di-cyclo-hexylthiophosphoryl) disulphide
Simultaneous thermal analysis
Polymeric gold(I) O,O′-di-cyclo-hexyl dithiophosphate
Molecular and supramolecular structure
Multinuclear 13C, 31P CP/MAS NMR spectroscopy
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Snippet ► Doubly-bridged binuclear gold(I) di-cyclo-hexyldithiophosphate comprising aurophilic bonds. ► Supramolecular self-organisation of polymeric chains involving...
Two novel compounds: polynuclear catena-poly[bis(μ₃-O,O′-di-cyclo-hexyldithiophosphato-S,S,S′)digold(I)] (AuAu) (1) and crystalline...
Two novel compounds: polynuclear catena-poly[bis( mu 3-O,O'-di-cyclo-hexyldithiophosphato-S,S,S')digol d(I)] (AuAu) (1) and crystalline...
Two novel compounds: polynuclear catena-poly[bis(3-O,O’-di-cyclo-hexyldithiophosphato-S,S,S’)digold(I)] (Au–Au) (1) and crystalline...
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SubjectTerms argon (noble gases)
Aurophilic bonding
Bis(O,O′-di-cyclo-hexylthiophosphoryl) disulphide
cadmium
Chemical bonds
Chemistry of Interfaces
Crystal structure
Displays
Fixation
Gold
Gränsytors kemi
hydrochloric acid
Molecular and supramolecular structure
Multinuclear 13C, 31P CP/MAS NMR spectroscopy
Neighbouring
Nuclear magnetic resonance
nuclear magnetic resonance spectroscopy
Polymeric gold(I) O,O′-di-cyclo-hexyl dithiophosphate
Simultaneous thermal analysis
spinning
Thermal analysis
thermal properties
X-ray diffraction
Title A fixation mode of gold from solutions using heterogeneous reaction of cadmium dicyclohexyl dithiophosphate with H[AuCl4]. Structural and (13C, 31P) CP/MAS NMR studies and thermal behaviour of crystalline polymeric gold(I) dicyclohexyl dithiophosphate and bis(dicyclohexylthiophosphoryl) disulphide
URI https://dx.doi.org/10.1016/j.molstruc.2012.08.052
https://search.proquest.com/docview/1221875266
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