Selective formation of the cis isomer of the nitridotechnetium(V) complex with 2,2′:6′,2″-terpyridine

T. Takayama; S. Oshikiri; T. Sekine; H. Kudo

doi:10.1007/BF02349519

Selective formation of the cis isomer of the nitridotechnetium(V) complex with 2,2′:6′,2″-terpyridine

T. Takayama, S. Oshikiri, T. Sekine, H. Kudo

Division of Developmental Research in Education Programs

Research output: Contribution to journal › Article › peer-review

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Abstract

The reaction of [TcNCl₂(PPh₃)₂] with 2,2′:6′,2″-terpyridine produced cis-[TcNCl₂(terpy)] selectively. The resulting complexes were characterized by ¹H NMR and IR spectroscopy. The geometries of the cis and trans isomers were estimated by theoretical calculations following a density functional method. The cis isomer is likely more stable than the trans one with respect to the trans influence of the nitrido ligand. Furthermore, the behavior of nitridotechnetium complexes in polar solvents was compared to Os-analogues.

Original language	English
Pages (from-to)	397-400
Number of pages	4
Journal	Journal of Radioanalytical and Nuclear Chemistry
Volume	239
Issue number	2
DOIs	https://doi.org/10.1007/BF02349519
Publication status	Published - 1999 Jan 1

ASJC Scopus subject areas

Analytical Chemistry
Nuclear Energy and Engineering
Radiology Nuclear Medicine and imaging
Pollution
Spectroscopy
Public Health, Environmental and Occupational Health
Health, Toxicology and Mutagenesis

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10.1007/BF02349519

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title = "Selective formation of the cis isomer of the nitridotechnetium(V) complex with 2,2′:6′,2″-terpyridine",

abstract = "The reaction of [TcNCl2(PPh3)2] with 2,2′:6′,2″-terpyridine produced cis-[TcNCl2(terpy)] selectively. The resulting complexes were characterized by 1H NMR and IR spectroscopy. The geometries of the cis and trans isomers were estimated by theoretical calculations following a density functional method. The cis isomer is likely more stable than the trans one with respect to the trans influence of the nitrido ligand. Furthermore, the behavior of nitridotechnetium complexes in polar solvents was compared to Os-analogues.",

author = "T. Takayama and S. Oshikiri and T. Sekine and H. Kudo",

year = "1999",

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doi = "10.1007/BF02349519",

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T1 - Selective formation of the cis isomer of the nitridotechnetium(V) complex with 2,2′:6′,2″-terpyridine

AU - Takayama, T.

AU - Oshikiri, S.

AU - Sekine, T.

AU - Kudo, H.

PY - 1999/1/1

Y1 - 1999/1/1

N2 - The reaction of [TcNCl2(PPh3)2] with 2,2′:6′,2″-terpyridine produced cis-[TcNCl2(terpy)] selectively. The resulting complexes were characterized by 1H NMR and IR spectroscopy. The geometries of the cis and trans isomers were estimated by theoretical calculations following a density functional method. The cis isomer is likely more stable than the trans one with respect to the trans influence of the nitrido ligand. Furthermore, the behavior of nitridotechnetium complexes in polar solvents was compared to Os-analogues.

AB - The reaction of [TcNCl2(PPh3)2] with 2,2′:6′,2″-terpyridine produced cis-[TcNCl2(terpy)] selectively. The resulting complexes were characterized by 1H NMR and IR spectroscopy. The geometries of the cis and trans isomers were estimated by theoretical calculations following a density functional method. The cis isomer is likely more stable than the trans one with respect to the trans influence of the nitrido ligand. Furthermore, the behavior of nitridotechnetium complexes in polar solvents was compared to Os-analogues.

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DO - 10.1007/BF02349519

M3 - Article

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VL - 239

SP - 397

EP - 400

JO - Journal of Radioanalytical and Nuclear Chemistry

JF - Journal of Radioanalytical and Nuclear Chemistry

SN - 0022-4081

IS - 2

ER -

Selective formation of the cis isomer of the nitridotechnetium(V) complex with 2,2′:6′,2″-terpyridine

Abstract

ASJC Scopus subject areas

UN SDGs

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