Employment and resurrection of surfactants in bipyridine promoted oxidation of butanal using bivalent copper at NTP

Research on Chemical Intermediates - A recent “Renaissance” has various fields of chemistry exploring processes that are more Earth-friendly One focus is to make kinetic experiments...     

Hetero-aromatic N-base-promoted oxidation of 4-chlorobenzyl alcohol by Cr(VI) in micellar media

Research on Chemical Intermediates - A little attempt has been made to get in touch with the green chemistry studying the successful occurrence of oxidation of 4-chlorobenzyl alcohol to...     

Crystal structure of a nucleoside analogue, 2′,3′-dideoxy-3′-fluoro-5-chlorocytidine

The title compound, 1-(2,3-dideoxy-3-fluoro--d-erythro pentofuranos-1-yl)-5-chlorocytosine, crystallises in the orthorhombic space groupP2₁2₁2₁ witha=5.142(1),b=14.177(2),c=15.721(2) Å,Z=4. The crystal structure was solved by the heavy atom method and refined by full-matrix least-squares method to a finalR value of 0.031 for 1629 unique observed reflections. The N-glycosidic torsion angle is –156.1(2)° and the sugar moiety is anti to the cytosine base. The sugar pucker is ₂ ³ T withP=178.2(1)° and=31(1)°. The atom 05 is in a +sc conformation with respect to the furanose ring. The molecular packing in the crystal is stabilized by N-HN, N-HO, O-HO hydrogen bonds and C-HO close contacts.     

Crystal structure of a nucleoside analog, 2′,3′-dideoxy-3′-azido-5-chlorocytidine

The title compound, l-(2,3-dideoxy-3-azido--D-erythro pentofuranos-1-yl)-5-chlorocytosine, crystallizes in the orthorhombic space groupP2₁2₁2₁ witha=5.840(1),b=13.780(1),c=15.396(2)Å,Z=4. The structure was solved by direct methods and refined by full-matrix least-squares calculations to a finalR value of 0.033 for 1688 unique observed reflections. The N-glycosidic torsion angle has a value of –160.8(1)°, in the and range. The sugar pucker is ₂ ³ T withP=180(1)° and=34(1)°. The C4–C5 conformation is +sc with =50.8(2)°. The azido group is nonlinear and oriented trans to the C3–C4 bond. The molecular packing in the crystalline space is stabilized by N-HN, N-HO, O-HO hydrogen bonds and C-HO close contacts.     

Crystal and molecular structure of 4-aminoacetyl-N-p-nitrophenylsulfanilamide

The crystal and molecular structure of 4-aminoacetyl-N-p-nitrophenylsulfanilamide (C₁₄H₁₃N₃O₅S), a derivative of sulfonamide, has been determined from X-ray diffraction data using Cu-K radiation. The compound crystallised in the monoclinic space groupP2₁/c, witha=12.258(9),b=7.339(5),c=16.359(9) Å,=98.84(4)°. The structure was solved by direct methods and refined by full-matrix least-squares to a finalR value of 0.047 with 2487 unique reflections. In packing, the molecules are found to be stabilised by N-H O hydrogen bonds.     

Thermoelectric power of RFeAsO (R = Ce,Pr, Nd,Sm and Gd)

Thermoelectric powers of a series of compounds RFeAsO (R = Ce, Pr, Nd, Sm and Gd) have been reported for temperatures ranging from 77 K up to room temperature. The behavior of S(T) in this temperature range can be divided into three regions. Every region has been fitted with mathematical functions of T. The physical significance of separate terms in the mathematical functions has been discussed. Some kind of universality has been observed between different members of the series.