About: The Zwitterion [8,8-μ-CH2O(CH3)-(1,2-C2B9H10)2-3,3-Co]0 as a Versatile Building Block To Introduce Cobalt Bis(Dicarbollide) Ion into Organic Molecules     Goto   Sponge   NotDistinct   Permalink

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  • The synthesis of a new bridged [8,8-μ-CH2O(CH3)-(1,2-C2B9H10)2-3,3-Co]0 derivative (2), arising from the acid-catalyzed reaction of cobalt bis(1,2-dicarbollide)(1) ion with formaldehyde, is reported. The proposed reaction path is supported by the isolation of side products including two zwitterionic compounds, the known bridged [8,8-μ-(CH3O)-(1,2-C2B9H10)2-3,3-Co]0 derivative (3), the new zwitterion [(8-(CH3)2O-1,2-C2B9H10)-(1,2-C2B9H11)-3,3-Co]0 (4), and two anionic compounds—the known [(8,8-Cl2-1,2-C2B9H10)2-3,3-Co] and the newly characterized dimethoxy derivative [(8,8-(CH3O)2-1,2-C2B9H10)2-3,3-Co] of the cobalt bis(dicarbollide) ion. Compound 2 serves as a versatile building block for the construction of zwitterionic derivatives, as exemplified by the synthesis of a series of compounds of general formulation [(8-X-CH2-1,2-C2B9H10)(8-CH3O-1,2-C2B9H10)-3,3-Co]0 (6). Compounds of type 6 bear organic end groups (X = NC5H5 (6a), C6H13NH2 (6b), 2-HOC2H4NH2 (6c), (C6H5)3P (6d)) adjacent to the cluster via a methylene spacer. The reactions with alcoholates or phenolates, demonstrated by the isolation of a derivative with X = 1-O(4-t-Bu-C6H4) (7–) in low yield, seem less advantageous due to the competing demethylation of the oxonium bridge in 2, which results in the preferential formation of the anion [8,8-μ-CH3O-(1,2-C2B9H10)2-3,3-Co] (8–). A similar side reaction was found to occur in the synthesis of a tetrasubstituted tert-butyl-calix[4]arene (9–), where one calixarene OH site was methylated producing the metallacarborane ion 8– instead of the bridge opening. The molecular structures of 6a,c–e, 8–, and 9– were determined by single-crystal X-ray diffraction analyses, and all compounds were characterized by high-resolution NMR (1H, 13C, and 11B) and mass spectrometry.
  • The synthesis of a new bridged [8,8-μ-CH2O(CH3)-(1,2-C2B9H10)2-3,3-Co]0 derivative (2), arising from the acid-catalyzed reaction of cobalt bis(1,2-dicarbollide)(1) ion with formaldehyde, is reported. The proposed reaction path is supported by the isolation of side products including two zwitterionic compounds, the known bridged [8,8-μ-(CH3O)-(1,2-C2B9H10)2-3,3-Co]0 derivative (3), the new zwitterion [(8-(CH3)2O-1,2-C2B9H10)-(1,2-C2B9H11)-3,3-Co]0 (4), and two anionic compounds—the known [(8,8-Cl2-1,2-C2B9H10)2-3,3-Co] and the newly characterized dimethoxy derivative [(8,8-(CH3O)2-1,2-C2B9H10)2-3,3-Co] of the cobalt bis(dicarbollide) ion. Compound 2 serves as a versatile building block for the construction of zwitterionic derivatives, as exemplified by the synthesis of a series of compounds of general formulation [(8-X-CH2-1,2-C2B9H10)(8-CH3O-1,2-C2B9H10)-3,3-Co]0 (6). Compounds of type 6 bear organic end groups (X = NC5H5 (6a), C6H13NH2 (6b), 2-HOC2H4NH2 (6c), (C6H5)3P (6d)) adjacent to the cluster via a methylene spacer. The reactions with alcoholates or phenolates, demonstrated by the isolation of a derivative with X = 1-O(4-t-Bu-C6H4) (7–) in low yield, seem less advantageous due to the competing demethylation of the oxonium bridge in 2, which results in the preferential formation of the anion [8,8-μ-CH3O-(1,2-C2B9H10)2-3,3-Co] (8–). A similar side reaction was found to occur in the synthesis of a tetrasubstituted tert-butyl-calix[4]arene (9–), where one calixarene OH site was methylated producing the metallacarborane ion 8– instead of the bridge opening. The molecular structures of 6a,c–e, 8–, and 9– were determined by single-crystal X-ray diffraction analyses, and all compounds were characterized by high-resolution NMR (1H, 13C, and 11B) and mass spectrometry. (en)
Title
  • The Zwitterion [8,8-μ-CH2O(CH3)-(1,2-C2B9H10)2-3,3-Co]0 as a Versatile Building Block To Introduce Cobalt Bis(Dicarbollide) Ion into Organic Molecules
  • The Zwitterion [8,8-μ-CH2O(CH3)-(1,2-C2B9H10)2-3,3-Co]0 as a Versatile Building Block To Introduce Cobalt Bis(Dicarbollide) Ion into Organic Molecules (en)
skos:prefLabel
  • The Zwitterion [8,8-μ-CH2O(CH3)-(1,2-C2B9H10)2-3,3-Co]0 as a Versatile Building Block To Introduce Cobalt Bis(Dicarbollide) Ion into Organic Molecules
  • The Zwitterion [8,8-μ-CH2O(CH3)-(1,2-C2B9H10)2-3,3-Co]0 as a Versatile Building Block To Introduce Cobalt Bis(Dicarbollide) Ion into Organic Molecules (en)
skos:notation
  • RIV/61388980:_____/12:00376238!RIV13-AV0-61388980
http://linked.open...avai/predkladatel
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • I, P(IAAX00320901), P(LC523), Z(AV0Z40320502), Z(MSM0021620857)
http://linked.open...iv/cisloPeriodika
  • 5
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 183140
http://linked.open...ai/riv/idVysledku
  • RIV/61388980:_____/12:00376238
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • boranes; carboranes; dicarbollides; X-ray diffraction; NMR (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • US - Spojené státy americké
http://linked.open...ontrolniKodProRIV
  • [85A534DA0668]
http://linked.open...i/riv/nazevZdroje
  • Organometallics
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 31
http://linked.open...iv/tvurceVysledku
  • Císařová, I.
  • Grüner, Bohumír
  • Plešek, Jaromír
  • Šícha, Václav
  • Böhmer, V.
http://linked.open...ain/vavai/riv/wos
  • 000301331200017
http://linked.open...n/vavai/riv/zamer
issn
  • 0276-7333
number of pages
http://bibframe.org/vocab/doi
  • 10.1021/om200938n
is http://linked.open...avai/riv/vysledek of
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