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231223s2007 xx ||||| 00| ||eng c |
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|a pubmed24n0566.xml
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|a (DE-627)NLM169863727
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|a (NLM)17455368
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Zeng, T
|e verfasserin
|4 aut
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|a Electron affinities of heavier phosphoryl and thiophosphoryl halides APX3 (A = O, S and X = Br, I)
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|c 2007
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|a Text
|b txt
|2 rdacontent
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|a ohne Hilfsmittel zu benutzen
|b n
|2 rdamedia
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|a Band
|b nc
|2 rdacarrier
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|a Date Completed 05.09.2007
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|a Date Revised 28.06.2007
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|a published: Print
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|a Citation Status PubMed-not-MEDLINE
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|a Copyright 2007 Wiley Periodicals, Inc.
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|a We carried out computational studies of OPX3 and SPX3 (X = Br and I) molecules and their corresponding anions using density functional theory, Møller-Plesset, and CCSD(T) methods with newly developed model core potentials (MCP). Reliabilities of the MCP were demonstrated by comparing experimental and calculated results. We computed the geometric structure, electron affinities, and electrostatic moments using systematic sequences of the dzp-, tzp-, and qzp-quality basis sets. Both C3v and Cs symmetries were assumed to ascertain that minima on the potential energy surface were found. Infrared and Raman frequencies were calculated and compared with available experimental data. Natural population analyses were performed and used to determine distribution of the extra electron in anions
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|a Journal Article
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|a Jamshidi, Z
|e verfasserin
|4 aut
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|a Mori, H
|e verfasserin
|4 aut
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|a Miyoshi, E
|e verfasserin
|4 aut
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|a Klobukowski, M
|e verfasserin
|4 aut
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|i Enthalten in
|t Journal of computational chemistry
|d 1984
|g 28(2007), 12 vom: 01. Sept., Seite 2027-33
|w (DE-627)NLM098138448
|x 1096-987X
|7 nnns
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| 773 |
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|g volume:28
|g year:2007
|g number:12
|g day:01
|g month:09
|g pages:2027-33
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|a GBV_ILN_350
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|a AR
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|d 28
|j 2007
|e 12
|b 01
|c 09
|h 2027-33
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