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with zwitterionic [3,3 0 -Co(8-C 4 H 8 O 2 -1,2-C 2 B 9 H 10 )(1 0 ,2 0 -C 2 B 9 H 11 )] [ 57 , 58 ]. Nucleo-
philic groups on the porphyrin macrocycle, such as hydroxy and pyridyl, efficiently
open the dioxane ring of [3,3 0 -Co(8-C 4 H 8 O 2 -1,2-C 2 B 9 H 10 )(1 0 ,2 0 -C 2 B 9 H 11 )], pro-
ducing porphyrins bearing Co(III) bis(dicarbollide) linked via a short PEG linkage
[ 57 - 62 ]. In the absence of these groups, metal-free porphyrins produce the
corresponding mono- and di-alkylated derivatives [ 61 ]. Since the Co(III) bis
(dicarbolide) is negatively charged, porphyrins 23 and 24 are octa- and tetra-
anionic, respectively. On the other hand, when pyridylporphyrins are used as the
starting materials for the ring opening reaction of [3,3 0 -Co(8-C 4 H 8 O 2 -1,2-C 2 B 9 H 10 )
(1 0 ,2 0 -C 2 B 9 H 11 )], zwitterionic carboranylporphyrins are formed [ 57 , 61 , 62 ].
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