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Cross-linking reactions, difficulty controlling

As mentioned previously, the main drawbacks of the thermal route to poly-borylborazine are (1) the presence of both direct intercyclic bonds and three-atom bridges between the rings, and (2) a difficulty in controlling the polycondensation rate. One solution we investigated to address these drawbacks is a route based on the room temperature reaction of /i-chloroborazine with trialkylaminoborane.31 32 We used 2-methylamino-4,6-dichloroborazine instead of 2,4,6-trichloroborazine to prepare a two-point polymer (scheme 4), which is theoretically less cross-linked. [Pg.133]


See other pages where Cross-linking reactions, difficulty controlling is mentioned: [Pg.1047]    [Pg.40]    [Pg.670]    [Pg.244]    [Pg.210]    [Pg.152]    [Pg.436]    [Pg.152]    [Pg.645]    [Pg.126]    [Pg.906]    [Pg.152]    [Pg.293]    [Pg.89]    [Pg.36]   
See also in sourсe #XX -- [ Pg.98 ]




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