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http://hdl.handle.net/10662/24299
Title: | N‐Bridged Acyclic Trimeric Poly‐Cyclodiphosphazanes: Highly Tuneable Cyclodiphosphazane Building Blocks. |
Authors: | Shi, Xiaoyan León, Félix Sim, Ying Quek, Shina Hum, Gavin Khoo, Yi Xin Joycelyn Xuan Ng, Zi Yang Par, Mian Chee Ong, How Singh, Varum K. Ganguly, Rakesh Clegg, Jack K. Díaz Álvarez, Jesús García, Felipe |
Keywords: | Compuestos acíclicos triméricos;Ciclodifosfazano;Moléculas terminales;Cambios;Afinidades cloruro;Acyclic trimeric cyclodiphosphazane;Cyclophosphazane;Terminal N(H)R moieties;Changes;Binding affinities |
Issue Date: | 2020 |
Publisher: | Wiley |
Abstract: | We have synthesized a completely new family of acyclic trimeric cyclodiphosphazane compounds comprising NH, NiPr, NtBu and NPh bridging groups. In addition, the first NH-bridged acyclic dimeric cyclophosphazane has been produced. The trimeric species display highly tuneable characteristics so that the distance between the terminal N(H)R moieties can be readily modulated by the steric bulk present in the bridging groups (ranging from &6 to &10 c). Moreover, these species exhibit pronounced topological changes when a weak non-bonding NH···p aryl interaction is introduced. Finally, the NH-bridged chloride binding affinities have been calculated and benchmarked along with the existing experimental data available for monomeric cyclodiphosphazanes. Our results underscore these species as promising hydrogen bond donors for supramolecular host–guest applications. |
URI: | http://hdl.handle.net/10662/24299 |
DOI: | 10.1002/anie.202008214 |
Appears in Collections: | DQOIN - Artículos |
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