[Dicyclohexyl(sulfanylidene)-λ5-phosphanyl]methanol
The title compound, [dicyclohexyl(sulfanylidene)-λ5 -phosphanyl]methanol, Cy2P(=S)CH2OH (1), was obtained from the reaction between [Cy2P(CH2OH)2]Cl with one molar equivalent of NaOH and an excess of elemental sulfur (powdered). Characterization was by a single-crystal X-ray structure determinatio...
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my.sunway.eprints.10692020-10-07T08:35:44Z http://eprints.sunway.edu.my/1069/ [Dicyclohexyl(sulfanylidene)-λ5-phosphanyl]methanol Henderson, William Okpareke, Obinna C. Ainnul H. S. Azizan, * Tiekink, Edward R. T. * QD Chemistry The title compound, [dicyclohexyl(sulfanylidene)-λ5 -phosphanyl]methanol, Cy2P(=S)CH2OH (1), was obtained from the reaction between [Cy2P(CH2OH)2]Cl with one molar equivalent of NaOH and an excess of elemental sulfur (powdered). Characterization was by a single-crystal X-ray structure determination as well as IR, and 1D-NMR (1H,13C{1H}, 31P{1H}), and 2D-NMR (DEPT-135 and HSQC) spectroscopy, ESI mass spectrometry, and elemental analysis. X-ray crystallography on Compound 1 shows the phosphorus atom to be tetrahedrally coordinated within a non-symmetric C3S donor set but with relatively minor distortions from the ideal geometry. In the molecular packing, hydroxyl-O–H· · · S(thione) hydrogen bonds led to supramolecular helical chains along the b-axis direction. MDPI 2019-07-02 Article PeerReviewed text en cc_by_nc_4 http://eprints.sunway.edu.my/1069/1/Tiekink%20Dicyclohexy%20.pdf Henderson, William and Okpareke, Obinna C. and Ainnul H. S. Azizan, * and Tiekink, Edward R. T. * (2019) [Dicyclohexyl(sulfanylidene)-λ5-phosphanyl]methanol. Molbank, 2019 (3). M1069. ISSN 1422-8599 http://doi.org/10.3390/M1069 doi:10.3390/M1069 |
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QD Chemistry Henderson, William Okpareke, Obinna C. Ainnul H. S. Azizan, * Tiekink, Edward R. T. * [Dicyclohexyl(sulfanylidene)-λ5-phosphanyl]methanol |
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The title compound, [dicyclohexyl(sulfanylidene)-λ5
-phosphanyl]methanol, Cy2P(=S)CH2OH (1), was obtained from the reaction between [Cy2P(CH2OH)2]Cl with one molar equivalent of NaOH and an excess of elemental sulfur (powdered). Characterization was by a single-crystal X-ray
structure determination as well as IR, and 1D-NMR (1H,13C{1H}, 31P{1H}), and 2D-NMR (DEPT-135 and HSQC) spectroscopy, ESI mass spectrometry, and elemental analysis. X-ray crystallography on Compound 1 shows the phosphorus atom to be tetrahedrally coordinated within a non-symmetric
C3S donor set but with relatively minor distortions from the ideal geometry. In the molecular packing, hydroxyl-O–H· · · S(thione) hydrogen bonds led to supramolecular helical chains along the b-axis direction. |
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Article |
author |
Henderson, William Okpareke, Obinna C. Ainnul H. S. Azizan, * Tiekink, Edward R. T. * |
author_facet |
Henderson, William Okpareke, Obinna C. Ainnul H. S. Azizan, * Tiekink, Edward R. T. * |
author_sort |
Henderson, William |
title |
[Dicyclohexyl(sulfanylidene)-λ5-phosphanyl]methanol |
title_short |
[Dicyclohexyl(sulfanylidene)-λ5-phosphanyl]methanol |
title_full |
[Dicyclohexyl(sulfanylidene)-λ5-phosphanyl]methanol |
title_fullStr |
[Dicyclohexyl(sulfanylidene)-λ5-phosphanyl]methanol |
title_full_unstemmed |
[Dicyclohexyl(sulfanylidene)-λ5-phosphanyl]methanol |
title_sort |
[dicyclohexyl(sulfanylidene)-λ5-phosphanyl]methanol |
publisher |
MDPI |
publishDate |
2019 |
url |
http://eprints.sunway.edu.my/1069/1/Tiekink%20Dicyclohexy%20.pdf http://eprints.sunway.edu.my/1069/ http://doi.org/10.3390/M1069 |
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