Electronic Raman transitions from the vanadium(III) hexa-aqua cation, in guanidinium vanadium sulphate

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Standard

Electronic Raman transitions from the vanadium(III) hexa-aqua cation, in guanidinium vanadium sulphate. / Spichiger, David; Carver, Graham; Dobe, Christopher; Bendix, Jesper; Tregenna-Piggott, Philip L.W.; Meier, Roland; Zahn, Gernot.

I: Chemical Physics Letters, Bind 337, Nr. 4-6, 06.04.2001, s. 391-397.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Spichiger, D, Carver, G, Dobe, C, Bendix, J, Tregenna-Piggott, PLW, Meier, R & Zahn, G 2001, 'Electronic Raman transitions from the vanadium(III) hexa-aqua cation, in guanidinium vanadium sulphate', Chemical Physics Letters, bind 337, nr. 4-6, s. 391-397. https://doi.org/10.1016/S0009-2614(01)00220-2

APA

Spichiger, D., Carver, G., Dobe, C., Bendix, J., Tregenna-Piggott, P. L. W., Meier, R., & Zahn, G. (2001). Electronic Raman transitions from the vanadium(III) hexa-aqua cation, in guanidinium vanadium sulphate. Chemical Physics Letters, 337(4-6), 391-397. https://doi.org/10.1016/S0009-2614(01)00220-2

Vancouver

Spichiger D, Carver G, Dobe C, Bendix J, Tregenna-Piggott PLW, Meier R o.a. Electronic Raman transitions from the vanadium(III) hexa-aqua cation, in guanidinium vanadium sulphate. Chemical Physics Letters. 2001 apr. 6;337(4-6):391-397. https://doi.org/10.1016/S0009-2614(01)00220-2

Author

Spichiger, David ; Carver, Graham ; Dobe, Christopher ; Bendix, Jesper ; Tregenna-Piggott, Philip L.W. ; Meier, Roland ; Zahn, Gernot. / Electronic Raman transitions from the vanadium(III) hexa-aqua cation, in guanidinium vanadium sulphate. I: Chemical Physics Letters. 2001 ; Bind 337, Nr. 4-6. s. 391-397.

Bibtex

@article{51fa547b315e4289af47228c4c03e306,
title = "Electronic Raman transitions from the vanadium(III) hexa-aqua cation, in guanidinium vanadium sulphate",
abstract = "Electronic Raman transitions (3A→3E(C3)) have been observed between the trigonally split components of the 3T1g(Oh) ground term of the vanadium(III) hexa-aqua cation in guanidinium vanadium sulphate hexa-hydrate. The magnitude of the trigonal field splitting is considerable, ~2720 cm-1, which is consistent with expectations based on the stereochemistry of the [V(OH2)6]3+ complex. It is shown that a satisfactory reproduction of the electronic Raman band profile can be obtained only by assuming a (3A⊕3E)⊗e vibronic coupling model.",
author = "David Spichiger and Graham Carver and Christopher Dobe and Jesper Bendix and Tregenna-Piggott, {Philip L.W.} and Roland Meier and Gernot Zahn",
year = "2001",
month = apr,
day = "6",
doi = "10.1016/S0009-2614(01)00220-2",
language = "English",
volume = "337",
pages = "391--397",
journal = "Chemical Physics Letters",
issn = "0009-2614",
publisher = "Elsevier",
number = "4-6",

}

RIS

TY - JOUR

T1 - Electronic Raman transitions from the vanadium(III) hexa-aqua cation, in guanidinium vanadium sulphate

AU - Spichiger, David

AU - Carver, Graham

AU - Dobe, Christopher

AU - Bendix, Jesper

AU - Tregenna-Piggott, Philip L.W.

AU - Meier, Roland

AU - Zahn, Gernot

PY - 2001/4/6

Y1 - 2001/4/6

N2 - Electronic Raman transitions (3A→3E(C3)) have been observed between the trigonally split components of the 3T1g(Oh) ground term of the vanadium(III) hexa-aqua cation in guanidinium vanadium sulphate hexa-hydrate. The magnitude of the trigonal field splitting is considerable, ~2720 cm-1, which is consistent with expectations based on the stereochemistry of the [V(OH2)6]3+ complex. It is shown that a satisfactory reproduction of the electronic Raman band profile can be obtained only by assuming a (3A⊕3E)⊗e vibronic coupling model.

AB - Electronic Raman transitions (3A→3E(C3)) have been observed between the trigonally split components of the 3T1g(Oh) ground term of the vanadium(III) hexa-aqua cation in guanidinium vanadium sulphate hexa-hydrate. The magnitude of the trigonal field splitting is considerable, ~2720 cm-1, which is consistent with expectations based on the stereochemistry of the [V(OH2)6]3+ complex. It is shown that a satisfactory reproduction of the electronic Raman band profile can be obtained only by assuming a (3A⊕3E)⊗e vibronic coupling model.

UR - http://www.scopus.com/inward/record.url?scp=0000613558&partnerID=8YFLogxK

U2 - 10.1016/S0009-2614(01)00220-2

DO - 10.1016/S0009-2614(01)00220-2

M3 - Journal article

AN - SCOPUS:0000613558

VL - 337

SP - 391

EP - 397

JO - Chemical Physics Letters

JF - Chemical Physics Letters

SN - 0009-2614

IS - 4-6

ER -

ID: 240003570