2007MacromoleculesRequires access

Modular Construction of Neutral and Anionic Carboranyl-Containing Carbosilane-Based Dendrimers

Arántzazu González‐Campo, Clara Viñas, Francesç Teixidor, Rosario Núñez, Reijo Sillanpää, Raikko Kivekäs

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Abstract

A modular construction of new carbosilane dendrimers, which contain four and eight peripheral carborane derivatives and propyl linkages between the C cluster and the Si atoms, has been developed using different methodologies. Regiospecific hydrosilylation of 1-C 6 H 5 -2-(CH 2 CH CH 2 )-l,2- closo -C 2 B 10 H 10 ( 1 ) and 1-CH 3 -2-(CH 2 CH CH 2 )-1,2- closo -C 2 B 10 H 10 ( 2 ) offers an efficient route to molecular precursors and building blocks that can provide both divergent and convergent strategies for dendritic growth. First generations of neutral carboranyl-containing dendrimers were constructed by two approaches: (a) a divergent approach via hydrosilylation of 1 and 2 with the first generation of a carbosilane dendrimer containing peripheral Si−H functions, Si[(CH 2 ) 2 (CH 3 ) 2 SiH] 4, 1G-H 4, to give dendrimers 7 and 8, respectively; (b) a convergent strategy, the growth of which was initiated with the groups that will become the periphery of the dendrimer. In the latter, the hydrosilylation of the allyl group in 1 and 2 with Me 2 HSiCl was carried out leading to the formation of 1-(CH 2 ) 3 SiCl-2-R-1,2- closo -C 2 B 10 H 10 [R = C 6 H 5 ( 3 ), CH 3 ( 4 )], and subsequent reduction with LiAlH 4 gave compounds 1-(CH 2 ) 3 SiH-2-R-1,2- closo -C 2 B 10 H 10 [R = C 6 H 5 ( 5 ), CH 3 ( 6 )], which were treated with tetravinylsilane or the core molecule to yield the first generation dendrimers, 7 and 8, with four carborane clusters. Next generation dendrimers were built up in a similar manner: (a) by the hydrosilylation using 1G-H 4 of the vinyl group in dendrons 9 and 10, which themselves have been prepared from the alkenylation of 3 and 4 with vinylmagnesium chloride; (b) by growing the carboranylsilane wedges 9 and 10 to a second generation and later assembling all to the core tetravinylsilane to obtain dendrimers 15 and 16 . In addition, another set of a second generation dendrimers containing eight carborane clusters were prepared by hydrosilylation of the vinyl groups in the dendrimer Si{(CH 2 ) 2 (CH 3 )Si[(CHCH 2 ) 2 ]} 4, 1G-Vi 8, with carboranylsilane dendrons 5 and 6, that contain Si−H functions. Degradation reaction of the peripheral closo -carboranes in dendrimers 7 and 8 using KOH/EtOH led to the formation of the corresponding polyanionic carbosilane dendrimers containing four peripheral nido -carborane clusters.

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A modular construction of new carbosilane dendrimers, which contain four and eight peripheral carborane derivatives and propyl linkages between the C cluster and the Si atoms, has been developed using different methodologies. Regiospecific hydrosilylation of 1-C 6 H 5 -2-(CH 2 CH CH 2 )-l,2- closo -C 2 B 10 H 10 ( 1 ) and 1-CH 3 -2-(CH 2 CH CH 2 )-1,2- closo -C 2 B 10 H 10 ( 2 ) offers an efficient route to molecular precursors and building blocks that can provide both divergent and convergent strategies for dendritic growth. First generations of neutral carboranyl-containing dendrimers were constructed by two approaches: (a) a divergent approach via hydrosilylation of 1 and 2 with the first generation of a carbosilane dendrimer containing peripheral Si−H functions, Si[(CH 2 ) 2 (CH 3 ) 2 SiH] 4, 1G-H 4, to give dendrimers 7 and 8, respectively; (b) a convergent strategy, the growth of which was initiated with the groups that will become the periphery of the dendrimer. In the latter, the hydrosilylation of the allyl group in 1 and 2 with Me 2 HSiCl was carried out leading to the formation of 1-(CH 2 ) 3 SiCl-2-R-1,2- closo -C 2 B 10 H 10 [R = C 6 H 5 ( 3 ), CH 3 ( 4 )], and subsequent reduction with LiAlH 4 gave compounds 1-(CH 2 ) 3 SiH-2-R-1,2- closo -C 2 B 10 H 10 [R = C 6 H 5 ( 5 ), CH 3 ( 6 )], which were treated with tetravinylsilane or the core molecule to yield the first generation dendrimers, 7 and 8, with four carborane clusters. Next generation dendrimers were built up in a similar manner: (a) by the hydrosilylation using 1G-H 4 of the vinyl group in dendrons 9 and 10, which themselves have been prepared from the alkenylation of 3 and 4 with vinylmagnesium chloride; (b) by growing the carboranylsilane wedges 9 and 10 to a second generation and later assembling all to the core tetravinylsilane to obtain dendrimers 15 and 16 . In addition, another set of a second generation dendrimers containing eight carborane clusters were prepared by hydrosilylation of the vinyl groups in the dendrimer Si{(CH 2 ) 2 (CH 3 )Si[(CHCH 2 ) 2 ]} 4, 1G-Vi 8, with carboranylsilane dendrons 5 and 6, that contain Si−H functions. Degradation reaction of the peripheral closo -carboranes in dendrimers 7 and 8 using KOH/EtOH led to the formation of the corresponding polyanionic carbosilane dendrimers containing four peripheral nido -carborane clusters.

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Available abstract

A modular construction of new carbosilane dendrimers, which contain four and eight peripheral carborane derivatives and propyl linkages between the C cluster and the Si atoms, has been developed using different methodologies. Regiospecific hydrosilylation of 1-C 6 H 5 -2-(CH 2 CH CH 2 )-l,2- closo -C 2 B 10 H 10 ( 1 ) and 1-CH 3 -2-(CH 2 CH CH 2 )-1,2- closo -C 2 B 10 H 10 ( 2 ) offers an efficient route to molecular precursors and building blocks that can provide both divergent and convergent strategies for dendritic growth. First generations of neutral carboranyl-containing dendrimers were constructed by two approaches: (a) a divergent approach via hydrosilylation of 1 and 2 with the first generation of a carbosilane dendrimer containing peripheral Si−H functions, Si[(CH 2 ) 2 (CH 3 ) 2 SiH] 4, 1G-H 4, to give dendrimers 7 and 8, respectively; (b) a convergent strategy, the growth of which was initiated with the groups that will become the periphery of the dendrimer. In the latter, the hydrosilylation of the allyl group in 1 and 2 with Me 2 HSiCl was carried out leading to the formation of 1-(CH 2 ) 3 SiCl-2-R-1,2- closo -C 2 B 10 H 10 [R = C 6 H 5 ( 3 ), CH 3 ( 4 )], and subsequent reduction with LiAlH 4 gave compounds 1-(CH 2 ) 3 SiH-2-R-1,2- closo -C 2 B 10 H 10 [R = C 6 H 5 ( 5 ), CH 3 ( 6 )], which were treated with tetravinylsilane or the core molecule to yield the first generation dendrimers, 7 and 8, with four carborane clusters. Next generation dendrimers were built up in a similar manner: (a) by the hydrosilylation using 1G-H 4 of the vinyl group in dendrons 9 and 10, which themselves have been prepared from the alkenylation of 3 and 4 with vinylmagnesium chloride; (b) by growing the carboranylsilane wedges 9 and 10 to a second generation and later assembling all to the core tetravinylsilane to obtain dendrimers 15 and 16 . In addition, another set of a second generation dendrimers containing eight carborane clusters were prepared by hydrosilylation of the vinyl groups in the dendrimer Si{(CH 2 ) 2 (CH 3 )Si[(CHCH 2 ) 2 ]} 4, 1G-Vi 8, with carboranylsilane dendrons 5 and 6, that contain Si−H functions. Degradation reaction of the peripheral closo -carboranes in dendrimers 7 and 8 using KOH/EtOH led to the formation of the corresponding polyanionic carbosilane dendrimers containing four peripheral nido -carborane clusters.

Key concepts: Hydrosilylation, Dendrimer, Chemistry, Carborane, Convergent synthesis, Stereochemistry, Polymer chemistry, Organic chemistry

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