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Boron Containing Mono- and Bis-carboranethiolate Derivatives of Respective Formula [(bipy)MCl(CBT)] and [(bipy)M(CBT)2] (M = PdII, PtII)
Synthesis and X-ray crystal structure of the species of formula [(bipy)MCl(CBT)]·0.5CH3CN (M = PdII, PtII) and [bipy)Pt(CBT)2] (CBT = m-carboranethiolate anion), of potential interest as anticancer agents in BNCT (boron neutron capture therapy). Detailed IR- and UV-visible spectra are also reported....
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Published in: | Inorganica Chimica Acta 2022-12, Vol.543, p.121160, Article 121160 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Synthesis and X-ray crystal structure of the species of formula [(bipy)MCl(CBT)]·0.5CH3CN (M = PdII, PtII) and [bipy)Pt(CBT)2] (CBT = m-carboranethiolate anion), of potential interest as anticancer agents in BNCT (boron neutron capture therapy). Detailed IR- and UV-visible spectra are also reported.
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•New Pd(II) and Pt(II) carboranethiolate derivatives of potential interest in BNCT. X-ray crystal structure. Physico-chemical properties.
Synthetic procedures are reported of the new “low molecular weight” mononuclear PdII and PtII derivatives of formula [(bipy)MCl(CBT)]·0.5CH3CN (M = PdII, PtII) and [(bipy)Pt(CBT)2] (CBT = m-carboranethiolate anion) evaluated of interest as potential anticancer agents in boron neutron capture therapy (BNCT). The structure of all three species has been elucidated by single-crystal X-ray work and further examined by IR and UV-visible spectral behavior. The detailed presentation of the spectral response for all of them in solution of low-donor non-aqueous solvents (CH3CN, DMF, DMSO) evidences the presence of a broad absorption in the region 400-500 nm, already previously observed for the species cis-[(bipy)Pd(CBT)2], this absorption interpreted as due to the presence of one or two metal-CBT environments in the related cis-structurally arranged mono- and bis-CBT derivatives. |
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ISSN: | 0020-1693 1873-3255 |
DOI: | 10.1016/j.ica.2022.121160 |