A modular approach to inorganic phosphazane macrocycles
Inorganic macrocycles, based on non-carbon backbones, present exciting synthetic challenges in the systematic assembly of inorganic molecules, as well as new avenues in host-guest and supramolecular chemistry. Here we demonstrate a new high-yielding modular approach to a broad range of trimeric and...
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| Main Authors: | , , , , , , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
21 April 2017
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| In: |
Angewandte Chemie
Year: 2017, Volume: 129, Issue: 31, Pages: 9215-9218 |
| ISSN: | 1521-3757 |
| DOI: | 10.1002/ange.201702558 |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/ange.201702558 Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/ange.201702558 
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| Author Notes: | Alex J. Plajer, Raúl García‐Rodríguez, Callum G.M. Benson, Peter D. Matthews, Andrew D. Bond, Sanjay Singh, Lutz H. Gade, and Dominic S. Wright |
| Summary: | Inorganic macrocycles, based on non-carbon backbones, present exciting synthetic challenges in the systematic assembly of inorganic molecules, as well as new avenues in host-guest and supramolecular chemistry. Here we demonstrate a new high-yielding modular approach to a broad range of trimeric and hexameric S- and Se-bridged inorganic macrocycles based on cyclophosphazane frameworks, using the building blocks [S=(H)P(μ-NR)]2. The method involves the in situ generation of the key intermediate [E (S )P(μ-NR)]22−(E=S, Se) dianion, which can be reacted with electrophilic [ClP(μ-NR)]2 to give PIII/PV hexameric rings or reacted with I2 to give trimeric PV variants. Important issues which are highlighted in this work are the competitive bridging ability of S versus Se in these systems and the synthesis of the first air-stable and chiral inorganic macrocycles. |
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| Item Description: | Gesehen am 15.12.2022 |
| Physical Description: | Online Resource |
| ISSN: | 1521-3757 |
| DOI: | 10.1002/ange.201702558 |