scholarly journals Synthesis, Properties, and Derivatization of Poly(dihydrogermane): A Germanium-based Polyethylene Analogue

Author(s):  
Haoyang Yu ◽  
Chuyi Ni ◽  
Alyxandra Thiessen ◽  
Ziqi Li ◽  
Jonathan G.C. Veinot

<div> <div> <div> <p>Polygermanes are germanium-based analogues of polyolefins and possess polymer backbones made up catenated Ge atoms. In the present contribution we report the preparation of a stable germanium polyethylene analogue – polydihydrogermane (i.e., (GeH2)n) – via two straightforward approaches that involve topotactic deintercalation of the CaGe Zintl phase. The resulting (GeH2)n possess morphologically dependent chemical and electronic properties and thermally decompose to yield amorphous hydrogenated Ge. We also show that the resulting (GeH2)n provide a platform from which functionalized polygermanes can be prepared via thermally-induced hydrogermylation-mediated pendant group substitution. This facile one-step derivatization reaction exploits Ge–H reactivity and opens the door to a wide array of tailored functional polygermanes. </p> </div> </div> </div>

2020 ◽  
Author(s):  
Haoyang Yu ◽  
Chuyi Ni ◽  
Alyxandra Thiessen ◽  
Ziqi Li ◽  
Jonathan G.C. Veinot

<div> <div> <div> <p>Polygermanes are germanium-based analogues of polyolefins and possess polymer backbones made up catenated Ge atoms. In the present contribution we report the preparation of a stable germanium polyethylene analogue – polydihydrogermane (i.e., (GeH2)n) – via two straightforward approaches that involve topotactic deintercalation of the CaGe Zintl phase. The resulting (GeH2)n possess morphologically dependent chemical and electronic properties and thermally decompose to yield amorphous hydrogenated Ge. We also show that the resulting (GeH2)n provide a platform from which functionalized polygermanes can be prepared via thermally-induced hydrogermylation-mediated pendant group substitution. This facile one-step derivatization reaction exploits Ge–H reactivity and opens the door to a wide array of tailored functional polygermanes. </p> </div> </div> </div>


2020 ◽  
Author(s):  
Haoyang Yu ◽  
Chuyi Ni ◽  
Alyxandra Thiessen ◽  
Ziqi Li ◽  
Jonathan G.C. Veinot

<div> <div> <div> <p>Polygermanes are germanium-based analogues of polyolefins and possess polymer backbones made up catenated Ge atoms. In the present contribution we report the preparation of a stable germanium polyethylene analogue – polydihydrogermane (i.e., (GeH2)n) – via two straightforward approaches that involve topotactic deintercalation of the CaGe Zintl phase. The resulting (GeH2)n possess morphologically dependent chemical and electronic properties and thermally decompose to yield amorphous hydrogenated Ge. We also show that the resulting (GeH2)n provide a platform from which functionalized polygermanes can be prepared via thermally-induced hydrogermylation-mediated pendant group substitution. This facile one-step derivatization reaction exploits Ge–H reactivity and opens the door to a wide array of tailored functional polygermanes. </p> </div> </div> </div>


2020 ◽  
Author(s):  
Haoyang Yu ◽  
Alyxandra Thiessen ◽  
Md Asjad Hossain ◽  
Marc Julian Kloberg ◽  
Bernhard Rieger ◽  
...  

<div><div><div><p>Covalently bonded organic monolayers play important roles in defining the solution processability, ambient stability, and electronic properties of two-dimensional (2D) materials such as Ge nanosheets (GeNSs); they also hold promise of providing avenues for the fabrication of future generation electronic and optical devices. Functionalization of GeNS normally involves surface moieties linked through covalent Ge−C bonds. In the present contribution we extend the scope of surface linkages to include Si−Ge bonding and present the first demonstration of heteronuclear dehydrocoupling of organosilanes to hydride-terminated GeNSs obtained from the deintercalation and exfoliation of CaGe2. We further exploit this new surface reactivity and demonstrated the preparation of directly bonded silicon quantum dot-Ge nanosheet hybrids.</p></div></div></div>


2012 ◽  
Vol 112 (10) ◽  
pp. 104107 ◽  
Author(s):  
P. Rauwel ◽  
E. Rauwel ◽  
C. Persson ◽  
M. F. Sunding ◽  
A. Galeckas

1998 ◽  
Vol 10 (12) ◽  
pp. 4025-4029 ◽  
Author(s):  
L. H. Yang ◽  
Charles D. Consorte ◽  
C. Y. Fong ◽  
J. E. Pask ◽  
E. Nabighian ◽  
...  

ChemInform ◽  
2009 ◽  
Vol 40 (44) ◽  
Author(s):  
Shamsuzzaman Shamsuzzaman ◽  
M. Gulfam Alam ◽  
Tabassum Siddiqui
Keyword(s):  

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