Alkoxysilanes
Alkoxysilanes are a class of organosilicon compounds characterized by the presence of silicon bonded to oxygen, which is in turn attached to an alkyl or aralkyl group. These materials exhibit excellent stability and reactivity due to their unique chemical structure, making them indispensable in various applications across industries.
Primarily used as coupling agents, alkoxysilanes enhance adhesion between organic polymers and inorganic substrates such as glass, metal, and ceramics. Their hydrolysis upon exposure to moisture forms a stable silanol layer, creating covalent bonds that improve material compatibility and durability.
Additionally, alkoxysilanes are employed in the preparation of coatings, sealants, and adhesives due to their ability to form strong chemical linkages with surfaces. They also find applications in the manufacture of fiber-reinforced composites, where they act as compatibilizers, improving the dispersion and interfacial bonding between fibers and matrix materials.
Overall, alkoxysilanes play a crucial role in enhancing product performance by promoting robust adhesion, improving wear resistance, and ensuring long-term stability under diverse environmental conditions.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Silane,(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)tripropoxy- | 521084-64-0 | C19H25F17O3Si |
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N-(3-Trimethoxysilylpropyl) Morpholine | 31024-54-1 | C10H23NO4Si |
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Aminophenyltrimethoxysilane | 33976-43-1 | C9H15NO3Si |
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2-Butenedioic acid(2E)-, 1,4-bis[3-(trimethoxysilyl)propyl] ester | 3371-62-8 | C16H32O10Si2 |
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1,3,6,9,12,15-Hexaoxa-2-silacycloheptadecane,2,2-dimethyl- | 83890-22-6 | C12H26O6Si |
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N-Methylaminopropyltrimethoxysilane | 3069-25-8 | C7H19NO3Si |
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N-(2-Aminoethyl)-3-aminopropylmethyldimethoxysilane | 3069-29-2 | C8H22N2O2Si |
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3-Aminopropylmethyldiethoxysilane | 3179-76-8 | C8H21NO2Si |
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Tetrabutyl orthosilicate | 4766-57-8 | C16H36O4Si |
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Tris(tert-butoxy)vinylsilane | 5356-88-7 | C14H30O3Si |
Related Literature
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Kathrin Kutlescha,Rhett Kempe New J. Chem., 2010,34, 1954-1960
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Sandip Gangadhar Balwe,Yeon Tae Jeong Org. Biomol. Chem., 2018,16, 1287-1296
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Xixi Li,Nanwei Zhu,Ruohan Li,Qinpu Zhang Anal. Methods, 2020,12, 3376-3381
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Zhonghua Xiang,Chuanqi Fang,Sanhua Leng,Dapeng Cao J. Mater. Chem. A, 2014,2, 7662-7665
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Yang Chen,Di Zhou,Zheyi Meng,Jin Zhai Chem. Commun., 2016,52, 10020-10023
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