English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

In an effort to introduce N-chloroarylsulphonamides of different oxydising strengths, sixteen sodium salts of N-chloro-mono- and di-substituted benzenesulphonamides of the configuration, 4- X-C 6 H 4 SO 2 NaNCl (where X = H; CH 3 ; C 2 H 5 ; F; Cl; Br; I or NO 2 ) and i-X, j-YC 6 H 3 SO 2 NaNCl (where i-X, j-Y = 2,3-(CH 3 ) 2 ; 2,4-(CH 3 ) 2 ; 2,5-(CH 3 ) 2 ; 2-CH 3 ,4-Cl; 2-CH 3 ,5-Cl; 3-CH 3 ,4-Cl; 2,4- Cl 2  or 3,4-Cl 2 ) are prepared, characterized through their infrared spectra in the solid state and NMR spectra in solution. The υ N-Cl  frequencies vary in the range 950 - 927 cm −1 . Effects of substitution in the benzene ring in terms of electron donating and electron withdrawing groups have been considered, and conclusions drawn. The chemical shifts of aromatic protons and carbon-13 in all the N-chloroarylsulphonamides have been calculated by adding substituent contributions to the shift of benzene. Considering the approximation employed the agreement between the calculated and experimental chemical shift values for different protons or carbon-13 is quite good. Effects of phenyl ring substitution on chemical shift values of both  1 H and  13 C are also graphically represented in terms of line diagrams.

zeitschrift für naturforschung a

Spectroscopic Studies with N-Chloroarylsulphonamides: IR and  1 H,  13 C and  23 Na Nmr Spectra of Sodium Salts of N-Chloro-Mono- and Di-Substituted-Benzenesulphonamides, 4-X-C 6 H 4 SO 2 NANCl (X = H; CH 3 ; C 2 H 5 ; F; Cl; Br; I or NO 2 ) and i-X, j-YC 6 H 3 SO 2 NANCl (i-X, j-Y = 2,3-(CH 3 ) 2 ; 2,4-(CH 3 ) 2 ; 2,5-(CH 3 ) 2 ; 2-CH 3 , 4-Cl; 2-CH 3 , 5-Cl; 3-CH 3 , 4-Cl; 2,4-Cl 2  or 3,4-Cl 2 )