Ring-Opening Radical Clock Reactions for Hybrid Organic−Silicon Surface Nanostructures:  A New Self-Directed Growth Mechanism and Kinetic Insights

Nano Letters ◽  
2004 ◽  
Vol 4 (2) ◽  
pp. 357-360 ◽  
Author(s):  
Xiao Tong ◽  
Gino A. DiLabio ◽  
Owen J. Clarkin ◽  
Robert A. Wolkow
2013 ◽  
Vol 21 (4) ◽  
pp. 4439 ◽  
Author(s):  
Cheng-Yun Zhang ◽  
Jian-Wu Yao ◽  
Chang-Qing Li ◽  
Qiao-Feng Dai ◽  
Sheng Lan ◽  
...  

Carbon ◽  
2009 ◽  
Vol 47 (3) ◽  
pp. 683-689 ◽  
Author(s):  
Teruhiko Ogata ◽  
Yoshio Tatamitani ◽  
Tetsu Mieno

2021 ◽  
Author(s):  
Xiao-Yu Zhang ◽  
Chao Ning ◽  
Ben Mao ◽  
Yin Wei ◽  
Min Shi

Classical cyclopropylcarbinyl radical clock reactions have been widely applied to conduct the mechanistic studies on probing radical process for a long time; however, alkylidenecyclopropanes, which have a similar molecular structure...


2009 ◽  
Vol 74 (16) ◽  
pp. 5850-5860 ◽  
Author(s):  
Götz Bucher ◽  
Atul A. Mahajan ◽  
Michael Schmittel
Keyword(s):  

2014 ◽  
Vol 50 (5) ◽  
pp. 527-529 ◽  
Author(s):  
Lauren M. Graham ◽  
Seungil Cho ◽  
Sung Kyoung Kim ◽  
Malachi Noked ◽  
Sang Bok Lee

1999 ◽  
Vol 576 ◽  
Author(s):  
Kamyar Rahimian ◽  
Douglas A. Loy

ABSTRACTSol-gel processing of materials is plagued by shrinkage during polymerization of the alkoxide monomers and processing (aging and drying) of the resulting gels. We have developed a new class of hybrid organic-inorganic materials based on the solventless ring-opening polymerization (ROP) of monomers bearing the 2,2,5,5-tetramethyl-2,5-disilaoxacyclopentyl group, which permits us to drastically reduce shrinkage in sol-gel processed materials. Because the monomers are polymerized through a chain growth mechanism catalyzed by base rather than the step growth mechanism normally used in sol-gel systems, hydrolysis and condensation products are entirely eliminated. Furthermore, since water is not required for hydrolysis, an alcohol solvent is not necessary. Monomers with two disilaoxacyclopentyl groups, separated by a rigid phenylene group or a more flexible alkylene group, were prepared through disilylation of the corresponding diacetylenes, followed by ring closure and hydrogenation. Anionic polymerization of these materials, either neat or with 2,2,5,5-tetramethyl-2,5-disila-1-oxacyclopentane as a copolymer, affords thermally stable transparent gels with no visible shrinkage. These materials provide an easy route to the introduction of sol-gel type materials in encapsulation of microelectronics, which we have successfully demonstrated.


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