The solv3rochromlccqu311ons dcscnbmg rbe cifects of solvent polar~ty/polwizab~hty (IT\*), solvenr hydrogen band donor acIdtry (a). and solbent hydrozcn bond xccptor bJsiaty (I?) have been determmed for scvcd Iluabundazole homologurs The s rosificlcnt ws iound to bc hnearly rclstcd to rhe Hammett o\*
Linear solvation energy relationships Solvent effects on some fluorescence probes
β Scribed by Mortimer J. Kamlet; Charles Dickinson; R.W. Taft
- Book ID
- 107732914
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- English
- Weight
- 477 KB
- Volume
- 77
- Category
- Article
- ISSN
- 0009-2614
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## Abstract The solvatochromic comparison method is used to unravel solvent polarity and hydrogen bonding effects on a variety of NMR spectral shifts and coupling constants. Solvent effects are rationalized in terms of the solvatochromic parameters Ο\*, Ξ΄, Ξ± and Ξ². Properties analyzed include ^19^F
A multiple linear regression analysis has been carried out using the Kamlet-Abboud-Taft solvatochromic parameters in order to quantify the solvent effects on the (17)O chemical shifts of methyl formate (MF). The influence of the solvents upon the carbonyl oxygen chemical shifts is smaller for MF tha
A multiple-linear-regression analysis (MLRA) has been carried to study intermolecular hydrogen bonding and as model out using the Kamlet-Abboud-Taft (KAT) solvatochromic pacompounds for the peptide bond (1-3). In particular, Kamrameters in order to elucidate and quantify the solvent effects let et a