Multicomponent Polymerization of Alkynes, Sulfonyl Azide, and Iminophosphorane at Room Temperature for the Synthesis of Hyperbranched Poly(phosphorus amidine)s

Synlett ◽  
2018 ◽  
Vol 29 (19) ◽  
pp. 2523-2528 ◽  
Author(s):  
Rongrong Hu ◽  
Ben Tang ◽  
Liguo Xu ◽  
Kou Yang

The construction of functional hyperbranched polymers with unique topological structures and distinct properties remains a great challenge. Multicomponent polymerization, as a fascinating polymer synthetic approach, has proved to be a powerful tool for the synthesis of polymers with diverse structures and multifunctionalities, which is a great advantage for the preparation of hyperbranched polymers. In this work, a multicomponent polymerization of alkynes, sulfonyl azide, and iminophosphorane is utilized for the construction of heteroatom-rich hyperbranched poly(phosphorus amidine)s with different topological structures and fluorescence response toward platinum group metal ions.

2017 ◽  
Vol 46 (9) ◽  
pp. 1422-1425 ◽  
Author(s):  
Su Ma ◽  
Kenji Funaki ◽  
Atsushi Miyazaki ◽  
Atsushi Muramatsu ◽  
Kiyoshi Kanie

1967 ◽  
Vol 22 (3) ◽  
pp. 268-269 ◽  
Author(s):  
Herschel Frye ◽  
Cecilia Luschak ◽  
Donald Chinn

The chelating tendencies of the alpha amino acids with platinum group metal ions are well known; with the dibasic acids, complexes have been reported involving palladium (II) and platinum (II) with both aspartic and glutamic acids. There is no mention of the successful synthesis of complexes between these acids and rhodium (III), however. This communication reports a method of preparation for these two complexes as well as an alternative method for the synthesis of the palladium (II) complex with aspartic acid. It is shown that the mole ratio of rhodium (III) to aspartate or glutamate is one to three, that the ligands act as bidentates, and that the aspartic acid complex. Infrared and elemental analytical data are given.


1985 ◽  
Vol 57 (12) ◽  
pp. 2403-2405 ◽  
Author(s):  
Krystyna. Brajter ◽  
Krystyna. Slonawska ◽  
James A. Cox

1989 ◽  
Vol 22 (3) ◽  
pp. 779-790 ◽  
Author(s):  
Krystyna Brajter ◽  
Krystyna Slonawska ◽  
James A. Cox

Molecules ◽  
2021 ◽  
Vol 26 (5) ◽  
pp. 1286
Author(s):  
Alessandra Garau ◽  
Giacomo Picci ◽  
Massimiliano Arca ◽  
Alexander J. Blake ◽  
Claudia Caltagirone ◽  
...  

This study investigates the coordination chemistry of the tetradentate pyridine-containing 12-membered macrocycles L1-L3 towards Platinum Group metal ions PdII, PtII, and RhIII. The reactions between the chloride salts of these metal ions and the three ligands in MeCN/H2O or MeOH/H2O (1:1 v/v) are shown, and the isolated solid compounds are characterized, where possible, by mass spectroscopy and 1H- and 13C-NMR spectroscopic measurements. Structural characterization of the 1:1 metal-to-ligand complexes [Pd(L1)Cl]2[Pd2Cl6], [Pt(L1)Cl](BF4), [Rh(L1)Cl2](PF6), and [Rh(L3)Cl2](BF4)·MeCN shows the coordinated macrocyclic ligands adopting a folded conformation, and occupying four coordination sites of a distorted square-based pyramidal and octahedral coordination environment for the PdII/PtII, and RhIII complexes, respectively. The remaining coordination site(s) are occupied by chlorido ligands. The reaction of L3 with PtCl2 in MeCN/H2O gave by serendipity the complex [Pt(L3)(m-1,3-MeCONH)PtCl(MeCN)](BF4)2·H2O, in which two metal centers are bridged by an amidate ligand at a Pt1-Pt2 distance of 2.5798(3) Å and feature one square-planar and one octahedral coordination environment. Density Functional Theory (DFT) calculations, which utilize the broken symmetry approach (DFT-BS), indicate a singlet d8-d8 PtII-PtII ground-state nature for this compound, rather than the alleged d9-d7 PtI-PtIII mixed-valence character reported for related dinuclear Pt-complexes.


2003 ◽  
Vol 42 (9) ◽  
pp. 3047-3056 ◽  
Author(s):  
David Amantia ◽  
Clayton Price ◽  
Michelle A. Shipman ◽  
Mark R. J. Elsegood ◽  
William Clegg ◽  
...  

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