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Exploiting the Ring Strain of Diphosphetanes: A Synthetic and Computational Approach towards 1,2,5‐Selenadiphospholanes

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Bibliographische Detailangaben
Zeitschriftentitel: ChemPlusChem
Personen und Körperschaften: Coburger, Peter, Aures, Richard, Schulz, Paulina, Hey‐Hawkins, Evamarie
In: ChemPlusChem, 84, 2019, 1, S. 2-2
Medientyp: E-Article
Sprache: Englisch
veröffentlicht:
Wiley
Schlagwörter:
author_facet Coburger, Peter
Aures, Richard
Schulz, Paulina
Hey‐Hawkins, Evamarie
Coburger, Peter
Aures, Richard
Schulz, Paulina
Hey‐Hawkins, Evamarie
author Coburger, Peter
Aures, Richard
Schulz, Paulina
Hey‐Hawkins, Evamarie
spellingShingle Coburger, Peter
Aures, Richard
Schulz, Paulina
Hey‐Hawkins, Evamarie
ChemPlusChem
Exploiting the Ring Strain of Diphosphetanes: A Synthetic and Computational Approach towards 1,2,5‐Selenadiphospholanes
General Chemistry
author_sort coburger, peter
spelling Coburger, Peter Aures, Richard Schulz, Paulina Hey‐Hawkins, Evamarie 2192-6506 2192-6506 Wiley General Chemistry http://dx.doi.org/10.1002/cplu.201800581 <jats:title>Abstract</jats:title><jats:p><jats:bold>Invited for this month's cover is the group of Prof. Evamarie Hey‐Hawkins from Leipzig University, Germany. The cover picture, designed by Dr. Christoph Selg, shows two pots on a crowded table planted with bulky</jats:bold> <jats:italic><jats:bold>tert</jats:bold></jats:italic>‐butyl groups symbolizing the phosphorus atoms in the strained ring system of a carborane‐substituted 1,2‐diphosphetane. However, selenium can still be inserted into the P−P bond, as reported by Hey‐Hawkins et al. in their present publication, which combines experimental and computational studies. Read the full text of the article at <jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="https://doi.org/10.1002/cplu.201800391">10.1002/cplu.201800391</jats:ext-link>.</jats:p> Exploiting the Ring Strain of Diphosphetanes: A Synthetic and Computational Approach towards 1,2,5‐Selenadiphospholanes ChemPlusChem
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title Exploiting the Ring Strain of Diphosphetanes: A Synthetic and Computational Approach towards 1,2,5‐Selenadiphospholanes
title_unstemmed Exploiting the Ring Strain of Diphosphetanes: A Synthetic and Computational Approach towards 1,2,5‐Selenadiphospholanes
title_full Exploiting the Ring Strain of Diphosphetanes: A Synthetic and Computational Approach towards 1,2,5‐Selenadiphospholanes
title_fullStr Exploiting the Ring Strain of Diphosphetanes: A Synthetic and Computational Approach towards 1,2,5‐Selenadiphospholanes
title_full_unstemmed Exploiting the Ring Strain of Diphosphetanes: A Synthetic and Computational Approach towards 1,2,5‐Selenadiphospholanes
title_short Exploiting the Ring Strain of Diphosphetanes: A Synthetic and Computational Approach towards 1,2,5‐Selenadiphospholanes
title_sort exploiting the ring strain of diphosphetanes: a synthetic and computational approach towards 1,2,5‐selenadiphospholanes
topic General Chemistry
url http://dx.doi.org/10.1002/cplu.201800581
publishDate 2019
physical 2-2
description <jats:title>Abstract</jats:title><jats:p><jats:bold>Invited for this month's cover is the group of Prof. Evamarie Hey‐Hawkins from Leipzig University, Germany. The cover picture, designed by Dr. Christoph Selg, shows two pots on a crowded table planted with bulky</jats:bold> <jats:italic><jats:bold>tert</jats:bold></jats:italic>‐butyl groups symbolizing the phosphorus atoms in the strained ring system of a carborane‐substituted 1,2‐diphosphetane. However, selenium can still be inserted into the P−P bond, as reported by Hey‐Hawkins et al. in their present publication, which combines experimental and computational studies. Read the full text of the article at <jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="https://doi.org/10.1002/cplu.201800391">10.1002/cplu.201800391</jats:ext-link>.</jats:p>
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author Coburger, Peter, Aures, Richard, Schulz, Paulina, Hey‐Hawkins, Evamarie
author_facet Coburger, Peter, Aures, Richard, Schulz, Paulina, Hey‐Hawkins, Evamarie, Coburger, Peter, Aures, Richard, Schulz, Paulina, Hey‐Hawkins, Evamarie
author_sort coburger, peter
container_issue 1
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description <jats:title>Abstract</jats:title><jats:p><jats:bold>Invited for this month's cover is the group of Prof. Evamarie Hey‐Hawkins from Leipzig University, Germany. The cover picture, designed by Dr. Christoph Selg, shows two pots on a crowded table planted with bulky</jats:bold> <jats:italic><jats:bold>tert</jats:bold></jats:italic>‐butyl groups symbolizing the phosphorus atoms in the strained ring system of a carborane‐substituted 1,2‐diphosphetane. However, selenium can still be inserted into the P−P bond, as reported by Hey‐Hawkins et al. in their present publication, which combines experimental and computational studies. Read the full text of the article at <jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="https://doi.org/10.1002/cplu.201800391">10.1002/cplu.201800391</jats:ext-link>.</jats:p>
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spelling Coburger, Peter Aures, Richard Schulz, Paulina Hey‐Hawkins, Evamarie 2192-6506 2192-6506 Wiley General Chemistry http://dx.doi.org/10.1002/cplu.201800581 <jats:title>Abstract</jats:title><jats:p><jats:bold>Invited for this month's cover is the group of Prof. Evamarie Hey‐Hawkins from Leipzig University, Germany. The cover picture, designed by Dr. Christoph Selg, shows two pots on a crowded table planted with bulky</jats:bold> <jats:italic><jats:bold>tert</jats:bold></jats:italic>‐butyl groups symbolizing the phosphorus atoms in the strained ring system of a carborane‐substituted 1,2‐diphosphetane. However, selenium can still be inserted into the P−P bond, as reported by Hey‐Hawkins et al. in their present publication, which combines experimental and computational studies. Read the full text of the article at <jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="https://doi.org/10.1002/cplu.201800391">10.1002/cplu.201800391</jats:ext-link>.</jats:p> Exploiting the Ring Strain of Diphosphetanes: A Synthetic and Computational Approach towards 1,2,5‐Selenadiphospholanes ChemPlusChem
spellingShingle Coburger, Peter, Aures, Richard, Schulz, Paulina, Hey‐Hawkins, Evamarie, ChemPlusChem, Exploiting the Ring Strain of Diphosphetanes: A Synthetic and Computational Approach towards 1,2,5‐Selenadiphospholanes, General Chemistry
title Exploiting the Ring Strain of Diphosphetanes: A Synthetic and Computational Approach towards 1,2,5‐Selenadiphospholanes
title_full Exploiting the Ring Strain of Diphosphetanes: A Synthetic and Computational Approach towards 1,2,5‐Selenadiphospholanes
title_fullStr Exploiting the Ring Strain of Diphosphetanes: A Synthetic and Computational Approach towards 1,2,5‐Selenadiphospholanes
title_full_unstemmed Exploiting the Ring Strain of Diphosphetanes: A Synthetic and Computational Approach towards 1,2,5‐Selenadiphospholanes
title_short Exploiting the Ring Strain of Diphosphetanes: A Synthetic and Computational Approach towards 1,2,5‐Selenadiphospholanes
title_sort exploiting the ring strain of diphosphetanes: a synthetic and computational approach towards 1,2,5‐selenadiphospholanes
title_unstemmed Exploiting the Ring Strain of Diphosphetanes: A Synthetic and Computational Approach towards 1,2,5‐Selenadiphospholanes
topic General Chemistry
url http://dx.doi.org/10.1002/cplu.201800581