Chemical Transformation: a Powerful Route to Metal Chalcogenide Nanowires

ChemInform ◽  
2007 ◽  
Vol 38 (9) ◽  
Author(s):  
Unyong Jeong ◽  
Pedro H. C. Camargo ◽  
Young Hwan Lee ◽  
Younan Xia
2017 ◽  
Vol 29 (7) ◽  
pp. 3219-3227 ◽  
Author(s):  
Gyeongbae Park ◽  
Jiwoo Lee ◽  
Sungmin Moon ◽  
Heeseung Yang ◽  
Anupam Giri ◽  
...  

2021 ◽  
Author(s):  
Chao Gu ◽  
Hou-Ming Xu ◽  
Shi-Kui Han ◽  
Min-Rui Gao ◽  
Shu-Hong Yu

This review summarizes the latest advances in design principles based on metastable metal chalcogenide nanomaterials (MCNs), together with corresponding soft chemical transformation rules to prepare or modify MCNs with novel or enhanced properties.


2006 ◽  
Vol 16 (40) ◽  
pp. 3893 ◽  
Author(s):  
Unyong Jeong ◽  
Pedro H. C. Camargo ◽  
Young Hwan Lee ◽  
Younan Xia

2015 ◽  
Vol 1 (10) ◽  
pp. e1500714 ◽  
Author(s):  
Yuan Yang ◽  
Kai Wang ◽  
Hai-Wei Liang ◽  
Guo-Qiang Liu ◽  
Mei Feng ◽  
...  

One-dimensional metal chalcogenide nanostructures are important candidates for many technological applications such as photovoltaic and thermoelectric devices. However, the design and synthesis of one-dimensional metal chalcogenide nanostructured materials with controllable components and properties remain a challenge. We report a general chemical transformation process for the synthesis of more than 45 kinds of one-dimensional alloyed/hybrid metal chalcogenide nanostructures inherited from mother template TexSey@Se core-shell nanowires with tunable compositions. As many as nine types of monometal chalcogenide alloy nanowires (including AgSeTe, HgSeTe, CuSeTe, BiSeTe, PbSeTe, CdSeTe, SbSeTe, NiSeTe, and CoSeTe) can be synthesized. Alloyed and hybrid nanowires integrated with two or more alloyed metal chalcogenide phases can also be prepared. The compositions of all of these metal chalcogenide nanowires are tunable within a wide range. This protocol provides a new general route for the controllable synthesis of a new generation of one-dimensional metal chalcogenide nanostructures.


1999 ◽  
Vol 09 (PR8) ◽  
pp. Pr8-313-Pr8-319
Author(s):  
I. S. Chuprakov ◽  
K. H. Dahmen

Synthesis ◽  
2021 ◽  
Author(s):  
Michio Kurosu ◽  
Katsuhiko Mitachi ◽  
David Mingle

Abstract(4,4′-Bisfluorophenyl)methoxymethyl (BFPM) group of uridine ureido nitrogen shows good relative stability in a variety of chemical transformation reactions for uridine. The BFPM group can be cleaved by 2% of TFA in CH2Cl2 without affecting the Boc group.


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