Research output: Contribution to journal › Article › peer-review
Photochemistry of cis,trans-[PtIV(en)(I)2(CH3COO)2] complex in aqueous solutions. / Glebov, E. M.; Pozdnyakov, I. P.; Magin, I. M. et al.
In: Russian Chemical Bulletin, Vol. 68, No. 8, 01.08.2019, p. 1532-1541.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Photochemistry of cis,trans-[PtIV(en)(I)2(CH3COO)2] complex in aqueous solutions
AU - Glebov, E. M.
AU - Pozdnyakov, I. P.
AU - Magin, I. M.
AU - Grivin, V. P.
AU - Plyusnin, V. F.
AU - Vasil’chenko, D. B.
AU - Zadesenets, A. V.
AU - Mel’nikov, A. A.
AU - Chekalin, S. V.
PY - 2019/8/1
Y1 - 2019/8/1
N2 - The photochemistry of aqueous solutions of the cis,trans-[PtIV(en)(I)2(CH3COO)2] complex (1) was studied by stationary photolysis, nanosecond laser flash photolysis and ultrafast kinetic spectroscopy in the time interval from hundreds of femtoseconds to minutes. It is shown that the multistage photolysis, including photochemical reactions of ligand exchange and photoreduction, involves in the fi rst step the formation of the cis-[IV(en)(I)2(CH3COO)2] complex with a quantum yield of 0.3 (irradiation at 282 nm). The further ligand exchange and photoreduction reactions occur with much lower quantum yields. The photochemical exchange of the acetate ion occurs in a time interval of ~100 ps with the much slower final step, being probably the acidic dissociation of the product. The key intermediate of the first step of the process was detected in the picosecond time range. Depending on the interpretation of the key intermediate nature, two possible mechanisms of the primary photochemical process are proposed.
AB - The photochemistry of aqueous solutions of the cis,trans-[PtIV(en)(I)2(CH3COO)2] complex (1) was studied by stationary photolysis, nanosecond laser flash photolysis and ultrafast kinetic spectroscopy in the time interval from hundreds of femtoseconds to minutes. It is shown that the multistage photolysis, including photochemical reactions of ligand exchange and photoreduction, involves in the fi rst step the formation of the cis-[IV(en)(I)2(CH3COO)2] complex with a quantum yield of 0.3 (irradiation at 282 nm). The further ligand exchange and photoreduction reactions occur with much lower quantum yields. The photochemical exchange of the acetate ion occurs in a time interval of ~100 ps with the much slower final step, being probably the acidic dissociation of the product. The key intermediate of the first step of the process was detected in the picosecond time range. Depending on the interpretation of the key intermediate nature, two possible mechanisms of the primary photochemical process are proposed.
KW - diiodo-Pt complexes
KW - photochemistry
KW - UV spectroscopy
KW - VISIBLE-LIGHT
KW - PLATINUM COMPLEX
KW - PHOTODYNAMIC THERAPY
KW - DNA
KW - PHOTOPHYSICS
KW - diiodo-Pt-IV complexes
KW - IRCL62-COMPLEX
KW - SPECTRA
KW - TRANS
UR - http://www.scopus.com/inward/record.url?scp=85070757516&partnerID=8YFLogxK
U2 - 10.1007/s11172-019-2588-y
DO - 10.1007/s11172-019-2588-y
M3 - Article
AN - SCOPUS:85070757516
VL - 68
SP - 1532
EP - 1541
JO - Russian Chemical Bulletin
JF - Russian Chemical Bulletin
SN - 1066-5285
IS - 8
ER -
ID: 21238577