Cargando…

O-Pivaloyl diphenyl­seleno­phosphinate

The title compound, C(17)H(19)O(2)PSe, was obtained in the reaction of the diphenyl­monoseleno­phosphinic acid ammonium salt with pivaloyl chloride. The P—Se bond length of 2.0769 (11) Å is normal, while the P—O bond length of 1.650 (3) Å is longer than in related O-alkyl and O-aryl derivatives. One...

Descripción completa

Detalles Bibliográficos
Autores principales: Cholewinski, Grzegorz, Chojnacki, Jaroslaw, Pikies, Jerzy, Rachon, Janusz
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968832/
https://www.ncbi.nlm.nih.gov/pubmed/21582571
http://dx.doi.org/10.1107/S1600536809009295
_version_ 1782189980525789184
author Cholewinski, Grzegorz
Chojnacki, Jaroslaw
Pikies, Jerzy
Rachon, Janusz
author_facet Cholewinski, Grzegorz
Chojnacki, Jaroslaw
Pikies, Jerzy
Rachon, Janusz
author_sort Cholewinski, Grzegorz
collection PubMed
description The title compound, C(17)H(19)O(2)PSe, was obtained in the reaction of the diphenyl­monoseleno­phosphinic acid ammonium salt with pivaloyl chloride. The P—Se bond length of 2.0769 (11) Å is normal, while the P—O bond length of 1.650 (3) Å is longer than in related O-alkyl and O-aryl derivatives. One phenyl ring is periplanar to the Se—P—C plane, while the dihedral angle between the two phenyl rings is ca 73°. The carbonyl group is in a synperiplanar position [torsion angle = 8.9 (6)°] to one of the methyl groups of the pivaloyl group. This is the first O-acyl derivative of diphenyl­monoseleno­phosphinic acid characterized by X-ray structural analysis.
format Text
id pubmed-2968832
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29688322010-12-30 O-Pivaloyl diphenyl­seleno­phosphinate Cholewinski, Grzegorz Chojnacki, Jaroslaw Pikies, Jerzy Rachon, Janusz Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(17)H(19)O(2)PSe, was obtained in the reaction of the diphenyl­monoseleno­phosphinic acid ammonium salt with pivaloyl chloride. The P—Se bond length of 2.0769 (11) Å is normal, while the P—O bond length of 1.650 (3) Å is longer than in related O-alkyl and O-aryl derivatives. One phenyl ring is periplanar to the Se—P—C plane, while the dihedral angle between the two phenyl rings is ca 73°. The carbonyl group is in a synperiplanar position [torsion angle = 8.9 (6)°] to one of the methyl groups of the pivaloyl group. This is the first O-acyl derivative of diphenyl­monoseleno­phosphinic acid characterized by X-ray structural analysis. International Union of Crystallography 2009-03-25 /pmc/articles/PMC2968832/ /pubmed/21582571 http://dx.doi.org/10.1107/S1600536809009295 Text en © Cholewinski et al. 2009 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Cholewinski, Grzegorz
Chojnacki, Jaroslaw
Pikies, Jerzy
Rachon, Janusz
O-Pivaloyl diphenyl­seleno­phosphinate
title O-Pivaloyl diphenyl­seleno­phosphinate
title_full O-Pivaloyl diphenyl­seleno­phosphinate
title_fullStr O-Pivaloyl diphenyl­seleno­phosphinate
title_full_unstemmed O-Pivaloyl diphenyl­seleno­phosphinate
title_short O-Pivaloyl diphenyl­seleno­phosphinate
title_sort o-pivaloyl diphenyl­seleno­phosphinate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968832/
https://www.ncbi.nlm.nih.gov/pubmed/21582571
http://dx.doi.org/10.1107/S1600536809009295
work_keys_str_mv AT cholewinskigrzegorz opivaloyldiphenylselenophosphinate
AT chojnackijaroslaw opivaloyldiphenylselenophosphinate
AT pikiesjerzy opivaloyldiphenylselenophosphinate
AT rachonjanusz opivaloyldiphenylselenophosphinate