About: Structure-Acidity-IR Spectra Correlations for p-Substituted N-Phenylsulfonylbenzamides     Goto   Sponge   NotDistinct   Permalink

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Description
  • Dissociation constants, IR absorption bands, Mulliken charges, heats of formation of p-substituted N-phenylsulfonylbenzamides and substituent constants were mutually correlated using mono and dual parameter correlations. The results showed that the factors describind the electronic structure and controlling the dissociation equilibrium and the IR spectra properties must be the same.
  • Dissociation constants, IR absorption bands, Mulliken charges, heats of formation of p-substituted N-phenylsulfonylbenzamides and substituent constants were mutually correlated using mono and dual parameter correlations. The results showed that the factors describind the electronic structure and controlling the dissociation equilibrium and the IR spectra properties must be the same. (en)
  • Disociační konstanty, IR vlnočty, Mullikenovy náboje a slučovací tepla p-substituovaných N-fenylsulfonylbenzamidů a sady substitučních konstant byly vzájemně korelovány s využitím jednoparametrových a dvouparametrových lineárních regresí. Výsledky ukazují na to, že faktory popisující elektronovou strukturu a faktory ovlivňující disociační rovnováhu a IR vlnočty jsou srovnatelné. (cs)
Title
  • Structure-Acidity-IR Spectra Correlations for p-Substituted N-Phenylsulfonylbenzamides
  • Structure-Acidity-IR Spectra Correlations for p-Substituted N-Phenylsulfonylbenzamides (en)
  • Korelace strukturních parametrů, disociačních konstant a IR vlnočtů pro p-substituované N-fenylsulfonylbenzamidy. (cs)
skos:prefLabel
  • Structure-Acidity-IR Spectra Correlations for p-Substituted N-Phenylsulfonylbenzamides
  • Structure-Acidity-IR Spectra Correlations for p-Substituted N-Phenylsulfonylbenzamides (en)
  • Korelace strukturních parametrů, disociačních konstant a IR vlnočtů pro p-substituované N-fenylsulfonylbenzamidy. (cs)
skos:notation
  • RIV/00216275:25310/04:00003450!RIV08-MSM-25310___
http://linked.open.../vavai/riv/strany
  • 213-222
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • S
http://linked.open...iv/cisloPeriodika
  • 4
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
  • 588549
http://linked.open...ai/riv/idVysledku
  • RIV/00216275:25310/04:00003450
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • Substituted N-phenylsulfonylbenzamides; IR spectral data; PM3 calculations; MP and DP correlations; substituent and solvent effects. (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • CH - Švýcarská konfederace
http://linked.open...ontrolniKodProRIV
  • [5BAA9F7D4A08]
http://linked.open...i/riv/nazevZdroje
  • Molecules
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 9
http://linked.open...iv/tvurceVysledku
  • Ludwig, Miroslav
  • Pařík, Patrik
  • Perjéssy, Alexander
  • Šusteková, Zora
  • Fabian, Walter M. F.
  • Loos, Dušan
issn
  • 1420-3049
number of pages
http://localhost/t...ganizacniJednotka
  • 25310
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