Arylthiolate coordination and reactivity at pseudotetrahedral nickel(II) centers: Modulation by noncovalent interactions

Swarup Chattopadhyay, Tapash Deb, Huaibo Ma, Jeffrey L. Petersen, Victor G. Young, Michael P. Jensen

Research output: Contribution to journalArticlepeer-review

20 Scopus citations


Five new pseudotetrahedral nickel(II) arylthiolate complexes Tp R.MeNi-SR′ [(TpR,Me)- = 2,2,2-κ3-hydridotris(3-R,5-methylpyrazolyl)borate; R = Me, R′ = C6H5 (Ph), 2,4,6-C6H 2(CH3)3 (Mes); R = Ph, R′ = C 6H5 (Ph), 2,4,6-C6H2(CH 3)3 (Mes), and 2,6-C6H3(CH 3)2 (Xyl)] were prepared by metathesis reactions of known chloride complexes with sodium arylthiolate salts in THF. The new products were fully characterized. The effect of increasing bulk of substituents at the proximal 3-pyrazolyl and ortho-thiolate positions represented in this series was evident in spectroscopic studies (UV-vis-NIR, 1H NMR) of the product complexes. Increased steric contact induced red-shifting of nickel-thiolate ligand to metal charge transfer (LMCT) bands and enhanced contact shifts of arylthiolate protons with the paramagnetic (S = 1) nickel(II) ion. These spectroscopic effects arise from structural distortion of the nickel(II)-thiolate bond revealed by X-ray crystal structure determinations of the structural extremes of the series, TpMe,MeNi-SPh and Tp Ph,MeNi-SXyl. The distortion consists of a significantly increased tilting of the Ni-S bond from an ideal trigonal axis and increased linearity of the Ni-S-R angle that alters covalency of the Ni-S coordinate bond. Reactivity of the nickel-thiolate linkage toward electrophilic alkylation with Mel is also significantly affected, showing enhanced rates according to two distinct competing mechanisms, direct bimolecular alkylation of intact complex and rate-limiting unimolecular dissociation of free thiolate. Possible biochemical relevance of these observations to tetrahedral nickel(II) centers in metalloenzymes is considered.

Original languageEnglish (US)
Pages (from-to)3384-3392
Number of pages9
JournalInorganic chemistry
Issue number8
StatePublished - Apr 21 2008


Dive into the research topics of 'Arylthiolate coordination and reactivity at pseudotetrahedral nickel(II) centers: Modulation by noncovalent interactions'. Together they form a unique fingerprint.

Cite this