2005
DOI: 10.1016/j.tetasy.2005.01.051
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Asymmetric heterogeneous carbene transfer catalyzed by optically active ruthenium spirobifluorenylporphyrin polymers

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Cited by 37 publications
(25 citation statements)
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“…On the other hand, it is difficult to obtain thick deposits from monomers with only one or two SBF units. For the compounds with only one unit, copolymerization was also performed with a small amount of SBF in order to improve the polymerization [60].…”
Section: Discussionmentioning
confidence: 99%
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“…On the other hand, it is difficult to obtain thick deposits from monomers with only one or two SBF units. For the compounds with only one unit, copolymerization was also performed with a small amount of SBF in order to improve the polymerization [60].…”
Section: Discussionmentioning
confidence: 99%
“…The 2-fluorenecarboxaldehyde is commercially available (Aldrich). The syntheses have been previously described in [55] for 1 and 1-RuCO, [56] for 2, 2-MnCl and 2-FeCl, [57] for 2-RuCO, [58] for 3, [59] for 3-MnCl, 5 and 5-MnCl, [60] for 4-RuCO, 6-RuCO. 2-RhI was prepared following a method previously described [64].…”
Section: Synthesis Of Monomersmentioning
confidence: 99%
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“…6,7 From a more fundamental point of view, the orthogonal configuration induced by the spiro carbon also allows to design shape persistent molecules with specific arrangements, which in turn has peculiar electronic consequences. 3,4,[8][9][10][11][12][13][14][15] In addition, the application field of the SBF scaffold is not only restricted to electronics and SBF has also found many other appealing applications as chiral ligand, [16][17][18][19] electropolymerizable building block, [20][21][22][23][24][25][26] homogeneous 27 and heterogeneous 23-25, 28, 29 catalysts or as building unit in coordination polymers, [30][31][32] clearly showing the versatility of this fragment. Sixteen positions of substitutions are available on the SBF backbone, eight on each fluorene unit (figure 1).…”
Section: Introductionmentioning
confidence: 99%
“…However, interest in 9,9'-spirobifluorenes, especially 9,9'-spirobifluorenebased oligomers, as well as polymers has recently switched to applications in molecular electronic devices for light emitting devices [11][12][13][14][15][16], hybrid porous solid [17] and catalysis [18].…”
Section: Introductionmentioning
confidence: 99%