"2"^^ . "9"^^ . . "0024-9297" . "290432" . "4"^^ . "Macromolecules" . . "Krupkov\u00E1, Alena" . . "RIV/67985858:_____/10:00343150" . "000277649500014" . . . . "Structural Defects in Polyallylcarbosilane Dendrimers and Their PolyolDerivatives Characterized by NMR and MALDI-TOF Mass Spectrometry"@en . "Structural Defects in Polyallylcarbosilane Dendrimers and Their PolyolDerivatives Characterized by NMR and MALDI-TOF Mass Spectrometry"@en . . . "10" . . . "Structural Defects in Polyallylcarbosilane Dendrimers and Their PolyolDerivatives Characterized by NMR and MALDI-TOF Mass Spectrometry" . "A series of polyallylcarbosilane dendrimers and carbosilane-based dendritic polyols up to third generation was analyzed by means of MALDI-TOF MS and multinuclear NMR to determine the character, origin, and number of structural defects. Several side reactions accompanying hydrosilylation, from which isomerization of terminal double bonds was the most abundant, were detected during the synthesis of carbosilane skeleton. Despite increased steric hindrance, internal double bonds react in subsequent addition reactions. Depending on the synthetic sequence applied, the retained reactivity of the internal double bonds can lead either to suppression of the defect in the next generation or to creation of more significant defects such as dendrimer dimers. Hydroboration of allyl groups using dicyclohexylborane proceeded with near quantitative conversion; a small amount of hydrolysis accompanying the following oxidation step producing nonreactive alkyl groups at the periphery was detected."@en . "P(LC06070), Z(AV0Z40500505), Z(AV0Z40720504)" . . "A series of polyallylcarbosilane dendrimers and carbosilane-based dendritic polyols up to third generation was analyzed by means of MALDI-TOF MS and multinuclear NMR to determine the character, origin, and number of structural defects. Several side reactions accompanying hydrosilylation, from which isomerization of terminal double bonds was the most abundant, were detected during the synthesis of carbosilane skeleton. Despite increased steric hindrance, internal double bonds react in subsequent addition reactions. Depending on the synthetic sequence applied, the retained reactivity of the internal double bonds can lead either to suppression of the defect in the next generation or to creation of more significant defects such as dendrimer dimers. Hydroboration of allyl groups using dicyclohexylborane proceeded with near quantitative conversion; a small amount of hydrolysis accompanying the following oxidation step producing nonreactive alkyl groups at the periphery was detected." . . "carbosilane dendrimers; maldi-tof ms; structural defects"@en . . "US - Spojen\u00E9 st\u00E1ty americk\u00E9" . . . . "\u010Cerm\u00E1k, Jan" . "Walterov\u00E1, Zuzana" . "[819FA4179C9C]" . . "RIV/67985858:_____/10:00343150!RIV11-MSM-67985858" . "Horsk\u00FD, Ji\u0159\u00ED" . "Structural Defects in Polyallylcarbosilane Dendrimers and Their PolyolDerivatives Characterized by NMR and MALDI-TOF Mass Spectrometry" . . "43" . .