Spectroscopic evidence for the direct coordination of the pertechnetate anion to the uranyl cation in [UO2(TcO4)(DPPMO 2)2]+

Andrew D. Sutton; Gordon H. John; Mark J. Sarsfield; Joanna C. Renshaw; Iain May; Leigh R. Martin; Andrew J. Selvage; David Collison; Madeleine Helliwell

doi:10.1021/ic049588r

Spectroscopic evidence for the direct coordination of the pertechnetate anion to the uranyl cation in [UO₂(TcO₄)(DPPMO ₂)₂]⁺

Andrew D. Sutton, Gordon H. John, Mark J. Sarsfield, Joanna C. Renshaw, Iain May^*, Leigh R. Martin, Andrew J. Selvage, David Collison, Madeleine Helliwell

^*Corresponding author for this work

Civil And Environmental Engineering

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

44 Citations (Scopus)

Abstract

We report the synthesis and structural characterization of [UO ₂-(ReO₄)(DPPMO₂)₂][ReO₄] and [UO₂(CI)(DPPMO₂)₂][CI] (where DPPMO ₂ = bis(diphenylphosphino)methane dioxide). In both complexes, the linear uranyl dication is coordinated to two bidentate DPPMO₂ ligands in the equatorial plane with one coordinated and one non-coordinated anion (either perrhenate or chloride). We have also prepared the pertechnetate analogue, and, through ³¹P and ⁹⁹Tc NMR, we have shown that the cation, [UO₂(TcO₄)(DPPMO₂) ₂]⁺, is stable in solution.

Original language	English
Pages (from-to)	5480-5482
Number of pages	3
Journal	Inorganic Chemistry
Volume	43
Issue number	18
Early online date	13 Aug 2004
DOIs	https://doi.org/10.1021/ic049588r
Publication status	Published - 6 Sept 2004

Keywords

spectroscopic evidence
direct coordination
[UO2(TcO4)(DPPMO2)2]+
pertechnetate anion
uranyl cation

Access to Document

10.1021/ic049588r

Cite this

@article{d085e7945a7c40f99815978321568f2b,

title = "Spectroscopic evidence for the direct coordination of the pertechnetate anion to the uranyl cation in [UO2(TcO4)(DPPMO 2)2]+",

abstract = "We report the synthesis and structural characterization of [UO 2-(ReO4)(DPPMO2)2][ReO4] and [UO2(CI)(DPPMO2)2][CI] (where DPPMO 2 = bis(diphenylphosphino)methane dioxide). In both complexes, the linear uranyl dication is coordinated to two bidentate DPPMO2 ligands in the equatorial plane with one coordinated and one non-coordinated anion (either perrhenate or chloride). We have also prepared the pertechnetate analogue, and, through 31P and 99Tc NMR, we have shown that the cation, [UO2(TcO4)(DPPMO2) 2]+, is stable in solution.",

keywords = "spectroscopic evidence , direct coordination, [UO2(TcO4)(DPPMO2)2]+, pertechnetate anion, uranyl cation",

author = "Sutton, {Andrew D.} and John, {Gordon H.} and Sarsfield, {Mark J.} and Renshaw, {Joanna C.} and Iain May and Martin, {Leigh R.} and Selvage, {Andrew J.} and David Collison and Madeleine Helliwell",

year = "2004",

month = sep,

day = "6",

doi = "10.1021/ic049588r",

language = "English",

volume = "43",

pages = "5480--5482",

journal = "Inorganic Chemistry",

issn = "0020-1669",

publisher = "American Chemical Society",

number = "18",

}

TY - JOUR

T1 - Spectroscopic evidence for the direct coordination of the pertechnetate anion to the uranyl cation in [UO2(TcO4)(DPPMO 2)2]+

AU - Sutton, Andrew D.

AU - John, Gordon H.

AU - Sarsfield, Mark J.

AU - Renshaw, Joanna C.

AU - May, Iain

AU - Martin, Leigh R.

AU - Selvage, Andrew J.

AU - Collison, David

AU - Helliwell, Madeleine

PY - 2004/9/6

Y1 - 2004/9/6

N2 - We report the synthesis and structural characterization of [UO 2-(ReO4)(DPPMO2)2][ReO4] and [UO2(CI)(DPPMO2)2][CI] (where DPPMO 2 = bis(diphenylphosphino)methane dioxide). In both complexes, the linear uranyl dication is coordinated to two bidentate DPPMO2 ligands in the equatorial plane with one coordinated and one non-coordinated anion (either perrhenate or chloride). We have also prepared the pertechnetate analogue, and, through 31P and 99Tc NMR, we have shown that the cation, [UO2(TcO4)(DPPMO2) 2]+, is stable in solution.

AB - We report the synthesis and structural characterization of [UO 2-(ReO4)(DPPMO2)2][ReO4] and [UO2(CI)(DPPMO2)2][CI] (where DPPMO 2 = bis(diphenylphosphino)methane dioxide). In both complexes, the linear uranyl dication is coordinated to two bidentate DPPMO2 ligands in the equatorial plane with one coordinated and one non-coordinated anion (either perrhenate or chloride). We have also prepared the pertechnetate analogue, and, through 31P and 99Tc NMR, we have shown that the cation, [UO2(TcO4)(DPPMO2) 2]+, is stable in solution.

KW - spectroscopic evidence

KW - direct coordination

KW - [UO2(TcO4)(DPPMO2)2]+

KW - pertechnetate anion

KW - uranyl cation

UR - http://www.scopus.com/inward/record.url?scp=4444381973&partnerID=8YFLogxK

U2 - 10.1021/ic049588r

DO - 10.1021/ic049588r

M3 - Article

C2 - 15332793

AN - SCOPUS:4444381973

SN - 0020-1669

VL - 43

SP - 5480

EP - 5482

JO - Inorganic Chemistry

JF - Inorganic Chemistry

IS - 18

ER -

Spectroscopic evidence for the direct coordination of the pertechnetate anion to the uranyl cation in [UO₂(TcO₄)(DPPMO ₂)₂]⁺

Abstract

Keywords

Access to Document

Other files and links

Fingerprint

Cite this