dc.creator |
Veinot, Alex J. |
|
dc.creator |
Hendsbee, Arthur D. |
|
dc.creator |
Masuda, Jason Douglas, 1977- |
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dc.date.accessioned |
2021-09-24T13:38:13Z |
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dc.date.available |
2021-09-24T13:38:13Z |
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dc.date.issued |
2017-04-21 |
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dc.identifier.issn |
2056-9890 |
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dc.identifier.uri |
http://library2.smu.ca/xmlui/handle/01/29932 |
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dc.description |
Published version |
en_CA |
dc.description.abstract |
<span>The title compound, C<sub>26</sub>H<sub>38</sub>ClN<sub>2</sub>OP, was synthesized by reacting phosphoryl chloride with <em>N</em>,<em>N</em><sup>′</sup>-bis­(2,6-diiso­propyl­phen­yl)ethane-1,2-di­amine in the presence of <em>N</em>-methyl­morpholine which acted as an auxilliary base to quench the HCl released as a by-product. The resultant <em>N</em>-heterocyclic phosphine five-membered ring adopts a half-chair conformation and features a tetra­coordinate P atom ligated by the chelating di­amine [P—N = 1.6348 (14) and 1.6192 (14) Å], one double-bonded O atom [P1—O1 = 1.4652 (12) Å] and one Cl atom [P1—Cl1 = 2.0592 (7) Å]. The sterically hindered 2,6-diiso­propyl­phenyl (Dipp) groups twist away from the central heterocycle, with torsion angles of −75.66 (19) and 83.39 (19)° for the P—N—C<sub>ar</sub>—C<sub>ar</sub> links. A number of intra­molecular C—H<sup>...</sup>N, C—H<sup>...</sup>O and C—H<sup>...</sup>Cl close contacts occur. In the crystal, mol­ecules are linked by C—H<sup>...</sup>O hydrogen bonds to generate [010] chains. C—H<sup>...</sup></span><sub><sup>Π </sup></sub>inter­actions are also observed. |
en_CA |
dc.description.provenance |
Submitted by Sherry Briere (sherry.briere@smu.ca) on 2021-09-24T13:38:13Z
No. of bitstreams: 1
Masuda_Jason_D_article_2017_c.pdf: 419001 bytes, checksum: 9bc9a96f41d769420e7874cbab2b64be (MD5) |
en |
dc.description.provenance |
Made available in DSpace on 2021-09-24T13:38:13Z (GMT). No. of bitstreams: 1
Masuda_Jason_D_article_2017_c.pdf: 419001 bytes, checksum: 9bc9a96f41d769420e7874cbab2b64be (MD5)
Previous issue date: 2017-04-21 |
en |
dc.language.iso |
en |
en_CA |
dc.publisher |
International Union of Crystallography |
en_CA |
dc.relation.uri |
https://doi.org/10.1107/S2056989017005825 |
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dc.rights |
<a rel="license" href="http://creativecommons.org/licenses/by/4.0/"><img alt="Creative Commons License" style="border-width:0" src="https://i.creativecommons.org/l/by/4.0/80x15.png" /></a> This work is licensed under a <a rel="license" href="http://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution 4.0 International License</a> |
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dc.subject.lcsh |
Crystallography |
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dc.subject.lcsh |
Heterocyclic compounds |
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dc.subject.lcsh |
Phosphorylation |
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dc.title |
Crystal structure of 2-chloro-1,3-bis(2,6-diiso- propylphenyl)-1,3,2-diazaphospholidine 2-oxide |
en_CA |
dc.type |
Text |
en_CA |
dcterms.bibliographicCitation |
Acta Crystallographica: Section E 73(5), 735–737. (2017) |
en_CA |