Comprehensive Vibrational Spectroscopic Investigation of trans,trans,trans-[Pt(N3)2(OH)2(py)2], a Pt(IV) Diazido Anticancer Prodrug Candidate

被引:22
作者
Vemooij, Robbin R. [1 ,2 ,3 ]
Joshi, Tanmaya [1 ]
Shaili, Evyenia [3 ]
Kubeil, Manja [1 ]
Appadoo, Dominique R. T. [4 ]
Izgorodina, Ekaterina I. [1 ]
Graham, Bim [5 ]
Sadler, Peter J. [3 ]
Wood, Bayden R. [1 ,2 ]
Spiccia, Leone [1 ]
机构
[1] Monash Univ, Sch Chem, Melbourne, Vic 3800, Australia
[2] Monash Univ, Ctr Biospectroscopy, Melbourne, Vic 3800, Australia
[3] Univ Warwick, Dept Chem, Gibbet Hill Rd, Coventry CV4 7AL, W Midlands, England
[4] Australian Synchrotron, 800 Blackburn Rd, Clayton, Vic 3168, Australia
[5] Monash Univ, Monash Inst Pharmaceut Sci, Melbourne, Vic 3052, Australia
基金
英国工程与自然科学研究理事会; 澳大利亚研究理事会;
关键词
FAR-INFRARED SPECTRA; PLATINUM(IV) COMPLEXES; RUTHENIUM COMPLEXES; PYRIDINE; DNA; TOXICITY; CRYSTALLINE; FREQUENCIES; GENERATION; CISPLATIN;
D O I
10.1021/acs.inorgchem.6b00476
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
We report a detailed study of a promising photo-activatable metal-based anticancer prodrug candidate, trans,trans,trans-[Pt(N-3)(2)(OH)(2)(py)(2)] (Cl; py = pyridine), using vibrational spectroscopic techniques. Attenuated total reflection Fourier transform infrared (ATR-FTIR), Raman, and synchrotron radiation far-IR (SR-FIR) spectroscopies were applied to obtain highly resolved ligand and Pt-ligand vibrations for Cl and its precursors (trans[Pt(N-3)(2)(py)(2)] (C2) and trans-[PtCl2(py)(2)] (C3)). Distinct IR- and Raman-active vibrational modes were assigned with the aid of density functional theory calculations, and trends in the frequency shifts as a function of changing Pt coordination environment were determined and detailed for the first time. The data provide the ligand and Pt-ligand (azide, hydroxide, pyridine) vibrational signatures for Cl in the mid- and far-IR region, which will provide a basis for the better understanding of the interaction of Cl with biomolecules.
引用
收藏
页码:5983 / 5992
页数:10
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