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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Woollins, John Derek
University of St Andrews
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (18/18 displayed)
- 2021Synthesis and structural characterization of Zn2+, Cd2+ and Hg2+ complexes with tripyrrolidinophosphine chalcogenidescitations
- 2021Synthetic and structural study of peri-substituted phosphine-arsinescitations
- 2019Synthesis, characterization, and structural properties of mercury(II), cadmium(II) and zinc(II) tripiperidinophosphine chalcogenide complexescitations
- 2018Synthesis, spectroscopic, and structural characterization of new functionalized gem-bisphosphonate complexes of tin(IV) chloride
- 2018A study of through-space and through-bond JPP coupling in a rigid nonsymmetrical bis(phosphine) and its metal complexescitations
- 2017Dye-sensitized solar cellscitations
- 2016Varying the flexibility of the aromatic backbone in half sandwich rhodium(III) dithiolato complexescitations
- 2016Synthesis, characterization and structures of cadmium(II) and mercury(II) complexes with bis(dipiperidinylphosphino)methylamine dichalcogenidescitations
- 2015Spirocyclic, macrocyclic and ladder complexes of coinage metals and mercury with dichalcogeno P2N2-supported anionscitations
- 2015Rhodium(III) and iridium(III) half-sandwich complexes with tertiary arsine and stibine ligandscitations
- 2015Peri-substituted phosphorus-tellurium systems – an experimental and theoretical investigation of the P∙∙∙Te through-space interactioncitations
- 2015Synthesis and properties of the heterospin (S1 = S2 = 1/2) radical-ion salt bis(mesitylene)molybdenum(I) [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidylcitations
- 2012Structure-Property Relationships in PtII Diimine-Dithiolate Nonlinear Optical Chromophores Based on Arylethylene-1,2-dithiolate and 2-Thioxothiazoline-4,5-dithiolatecitations
- 2004Ruthenium(II) carbonyl complexes containing tertiary phosphine chalcogenide ligands of the type Ph 3 PX; X=O, S, Secitations
- 2003Phosphorus-selenium heterocycles from the tetraphospholane (PhP) 4 CH 2
- 2001Synthesis of chelate complexes and the dichalcogen derivatives of the unsymmetrical diphosphine ligand Ph 2 PNHC 6 H 4 PPh 2 . Molecular Structure of [PtCl 2 (Ph 2 PNHC 6 H 4 PPh 2 )]·0.75dmso·0.75CHCl 3citations
- 2001Bridge cleavage of transition metal dimers by chelating S,N ligands. X-ray crystal structure of [Pd{SPPh 2 N=C(NH2)NH-S,N}(3-C3H5)]
- 2001The Evolution, Chemistry and Applications of Homogeneous Liquid Redox Sulfur Recovery Techniques
Places of action
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article
Synthesis and structural characterization of Zn2+, Cd2+ and Hg2+ complexes with tripyrrolidinophosphine chalcogenides
Abstract
Six new complexes of zinc(II), cadmium(II) and mercury(II) chlorides with tripyrrolidinophosphine chalcogenides of the types [MCl<sub>2</sub>(Pyrr<sub>3</sub>PE)<sub>2</sub>] (M = Zn, E = S (1) or E = Se (2); M = Cd, E = S (3) or E = Se (4)) and [{HgCl(Pyrr<sub>3</sub>PE)}<sub>2</sub>(µ-Cl)<sub>2</sub>] (E = S (5) or Se (6)) have been prepared in yields of 66-92% by reaction of the ligands with metal chloride in ethanol and characterized by 1H and 31P NMR, IR, elemental analysis, conductivity, and single crystal X-ray diffraction analysis. The results show that the complexes are pseudo-tetrahedral containing coordinated chloride ions. Interestingly, the X-ray studies reveal that while the title ligands produce dinuclear complexes with Hg, their Cd and Zn complexes are mononuclear. The tetrahedral bond angles vary from 85.69(5)° to 126.25(4)° in dinuclear complexes 5 and 6 and from 93.51(3)° to 117.38(3)° in mononuclear species 2-4. The E = S bond lengths are in the range 1.999(9)-2.198(2) Å. The coordination properties of the title ligands are discussed and compared to those obtained for their bulkier counterparts.