Polymer Zwitterions with Phosphonium Cations

Author(s):  
Marcel U. Brown ◽  
Alexandria Triozzi ◽  
Todd Emrick
Keyword(s):  
2017 ◽  
Vol 46 (46) ◽  
pp. 16216-16227 ◽  
Author(s):  
Alejandro G. Barrado ◽  
Julia M. Bayne ◽  
Timothy C. Johnstone ◽  
Christian W. Lehmann ◽  
Douglas W. Stephan ◽  
...  

Two strategies were used to prepare dicationic phosphonium cations.


CrystEngComm ◽  
2020 ◽  
Vol 22 (1) ◽  
pp. 52-60 ◽  
Author(s):  
Sze Le Loh ◽  
Alexandre N. Sobolev ◽  
Siew Huah Lim ◽  
Irene Ling

The interplay of different organic dications substituted at ortho- or meta-positions on the bis(methylene)phenyl ring and p-sulfonatocalix[4]arene, along with phosphonium cations and hydrated lanthanides affords new fascinating self-assembled structures.


2018 ◽  
Vol 54 (88) ◽  
pp. 12467-12470 ◽  
Author(s):  
J. M. Bayne ◽  
V. Fasano ◽  
K. M. Szkop ◽  
M. J. Ingleson ◽  
D. W. Stephan

The water/base intolerance of the previously reported electrophilic phosphonium cations has been overcome by replacing the labile electron-withdrawing groups generally attached to phosphorus (e.g. –F, –OAr, –CF3) with methyl groups.


2017 ◽  
Vol 46 (45) ◽  
pp. 15961-15961
Author(s):  
Daniel Upmann ◽  
Peter G. Jones

Correction for ‘Synthesis and X-ray structural characterization of the (chlorochalcogeno)phosphonium cations R2R′PSCl+ and R2R′PSeCl+ as their AuCl4− salts’ by Daniel Upmann and Peter G. Jones, Dalton Trans., 2013, 42, 7526–7528.


2008 ◽  
Vol 63 (7) ◽  
pp. 853-859 ◽  
Author(s):  
Hubert Schmidbaur

Recent theoretical studies of the molecular and electronic structure of tetra[(phosphine)gold(I)]- phosphonium cations, [(H3PAu)4P]+, gave contradictory results favoring either a classical tetrahedral or a unique square-pyramidal structure of the PAu4 unit. A tetrahedral structure had previously been confirmed for the corresponding ammonium cations [(Ph3PAu)4N]+, while a square-pyramidal structure was discovered for the corresponding arsonium cations [(Ph3PAu)4As]+, but there is as yet no unequivocal experimental evidence for the structure of phosphonium cations like [(Ph3PAu)4P]+ in an innocent environment. - In this account the structural chemistry of this class of onium salts and related species is reviewed. The data accumulated to date provide virtually compelling evidence that the phosphonium cations should have a ground state with a square pyramidal PAu4 core unit, provided that no external constraints are imposed. For large central elements (P, As), aurophilic interactions appear to drive the reorganization from tetrahedral to square-pyramidal skeletons in which a maximum number of short Au---Au contacts can be maintained. For the small central element N, similar interactions are already realized in the tetrahedral structure.


2011 ◽  
Vol 21 (21) ◽  
pp. 7640 ◽  
Author(s):  
Vanessa Armel ◽  
David Velayutham ◽  
Jiazeng Sun ◽  
Patrick C. Howlett ◽  
Maria Forsyth ◽  
...  

2018 ◽  
Vol 54 (79) ◽  
pp. 11164-11167 ◽  
Author(s):  
Tristan D. Harrison ◽  
Paul J. Ragogna ◽  
Elizabeth R. Gillies

Hydrogels containing phosphonium cations were synthesized and demonstrated to electrostatically bind and release anionic drug molecules depending on their structures.


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