Back to Search Start Over

Crucial Influence of the Intramolecular Hydrogen Bond on the Coordination Mode of RC(S)NHP(S)(O iPr)2 in Homoleptic Complexes with NiII.

Authors :
Babashkina, Maria G.
Safin, Damir A.
Srebro, Monika
Kubisiak, Piotr
Mitoraj, Mariusz P.
Bolte, Michael
Garcia, Yann
Source :
European Journal of Inorganic Chemistry. Feb2013, Vol. 2013 Issue 4, p545-555. 11p.
Publication Year :
2013

Abstract

Reaction of the deprotonated N-thiophosphorylated thioureas RC(S)NHP(S)(O iPr)2 [R = EtNH ( HLI), iPrNH ( HLII), Et2N ( HLIII), 2,5-Me2C6H3NH ( HLIV), 4-Me2NC6H4NH ( HLV)] with NiII leads to complexes of the formula [NiLI-V2]. The molecular structures of the complexes in the solid were elucidated by single-crystal X-ray diffraction analysis. In the complexes, the metal atom is found to be in a square-planar trans- N2 S2 ( [NiLII,IV2]) environment formed by the C=S sulfur atoms and the P-N nitrogen atoms, or in a square-planar trans- S2 S′2 ( [NiLI,III2]) environment formed by the C=S and P=S sulfur atoms of two deprotonated ligands. Reaction of deprotonated N-thiophosphorylated thiourea HLV with NiCl2 leads to violet [Ni(L-1,3- N, S)2] or dark violet [Ni(L-1,5- S, S′)2]·(CH3)2C=O crystals that were isolated by recrystallization from a mixture of CH2Cl2 or acetone, respectively, and n-hexane. DFT calculations confirmed that the [Ni(LI,II,IV,V- N, S)2] conformers are more stable (by 5-7 kcal/mol) than [Ni(LI,II,IV,V- S, S′)2], whereas [Ni(LIII- N, S)2] is less stable (by 7-9 kcal/mol) than [Ni(LIII- S, S′)2]. The main reason for higher stability of the 1,3- N, S versus 1,5- S, S′ isomers is the formation of intramolecular N-H ···S=P hydrogen bonds. The same hydrogen bonds are impossible in complex [NiLIII2]. In solution, complex [NiLIII2] has revealed an exclusively 1,5- S, S′ coordination, whereas compounds [NiLI,II,IV,V2] reveal at least two isomers in the 1H and 31P{1H} NMR spectra. The major species is assigned to the 1,3- N, S-coordinated isomer, and the minor signals are assigned to the 1,5- S, S′ isomer, which was confirmed by UV/Vis spectroscopic results. The electrochemical measurements reveal reversible one-electron reduction and irreversible oxidations both assigned to ligand-centred processes. Ligand-based oxidation processes agree well with TD-DFT results. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14341948
Volume :
2013
Issue :
4
Database :
Academic Search Index
Journal :
European Journal of Inorganic Chemistry
Publication Type :
Academic Journal
Accession number :
85029269
Full Text :
https://doi.org/10.1002/ejic.201200890