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Description
  • The tautomeric behaviour of individual compounds is therefore strongly affected by the nature of the substituent, as assessed via NMR spectroscopy in terms of tautomerisation constants K-T = C-Z2/C-N2 (where C-Z2 and C-N2 are equilibrium concentrations of Z2 and N2 forms in a given solvent). Individual tautomers were characterised by B-11 and H-1 NMR spectroscopy and the structure of the monomethylated N2b tautomer was determined by an X-ray diffraction study.
  • The tautomeric behaviour of individual compounds is therefore strongly affected by the nature of the substituent, as assessed via NMR spectroscopy in terms of tautomerisation constants K-T = C-Z2/C-N2 (where C-Z2 and C-N2 are equilibrium concentrations of Z2 and N2 forms in a given solvent). Individual tautomers were characterised by B-11 and H-1 NMR spectroscopy and the structure of the monomethylated N2b tautomer was determined by an X-ray diffraction study. (en)
Title
  • Synthesis of C-substituted t-BuNH-8,9-R,R '-nido-7,8,9-C3B8H9 (R,R ' = H, H;MeH;Me,Me;Ph,H and Ph,Ph) tricarbollide compounds and their tautomeric conversions. Effect of substituents on tautomeric equilibria between neutral and zwitterionic forms
  • Synthesis of C-substituted t-BuNH-8,9-R,R '-nido-7,8,9-C3B8H9 (R,R ' = H, H;MeH;Me,Me;Ph,H and Ph,Ph) tricarbollide compounds and their tautomeric conversions. Effect of substituents on tautomeric equilibria between neutral and zwitterionic forms (en)
skos:prefLabel
  • Synthesis of C-substituted t-BuNH-8,9-R,R '-nido-7,8,9-C3B8H9 (R,R ' = H, H;MeH;Me,Me;Ph,H and Ph,Ph) tricarbollide compounds and their tautomeric conversions. Effect of substituents on tautomeric equilibria between neutral and zwitterionic forms
  • Synthesis of C-substituted t-BuNH-8,9-R,R '-nido-7,8,9-C3B8H9 (R,R ' = H, H;MeH;Me,Me;Ph,H and Ph,Ph) tricarbollide compounds and their tautomeric conversions. Effect of substituents on tautomeric equilibria between neutral and zwitterionic forms (en)
skos:notation
  • RIV/61388980:_____/10:00356973!RIV11-MSM-61388980
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(LC523), Z(AV0Z40320502), Z(MSM0021620857)
http://linked.open...iv/cisloPeriodika
  • 17
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
  • 291525
http://linked.open...ai/riv/idVysledku
  • RIV/61388980:_____/10:00356973
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • magnetic-resonance-spectroscopy; derivatives; series (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [86F23D65A2FB]
http://linked.open...i/riv/nazevZdroje
  • Dalton Transactions
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
  • 39
http://linked.open...iv/tvurceVysledku
  • Bakardjiev, Mario
  • Císařová, I.
  • Holub, Josef
  • Štíbr, Bohumil
http://linked.open...ain/vavai/riv/wos
  • 000276633000019
http://linked.open...n/vavai/riv/zamer
issn
  • 1477-9226
number of pages
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