Structural and spectroscopic investigation of 1-amino-2,4-dinitrobenzenes
✍ Scribed by M. Virginia Remedi; Elba I. Buján; Ricardo Baggio; María Teresa Garland
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 104 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0894-3230
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✦ Synopsis
The crystal structures of 1-pyrrolidino-2,4-dinitrobenzene (3) and 1-morpholino-2,4-dinitrobenzene (4) were determined by single-crystal x-ray diffraction and the structures in solution were investigated by UV-visible spectrophotometry and 13 C and 1 H NMR spectrosccopy. Compound 4 crystallizes in the monoclinic space group P2 1 / n with one independent molecule per asymmetric unit and 3 crystallizes in triclinic P-1 with three independent molecules per asymmetric unit. Rotation of the o-nitro group and of the amino group out of the aromatic plane was observed in both the solid state and in solution for both compounds.
📜 SIMILAR VOLUMES
The organotin(IV) chlorides R n SnCl 4 -n (n=2, R = n Bu or Ph; and n=3, R= Ph) react with 2-amino-1-cyclopentene-1-carbodithioic acid (ACDA) to give [Ph 2 SnCl(ACDA)] (1), [Ph 2 Sn(ACDA) 2 ] (2), [Ph 3 Sn(ACDA)] (3) and [Bu 2 Sn(ACDA) 2 ] (4). The new complexes have been characterized by elemental
l-fluoro-2,4-dinitrophenyl-5-L-alanine amide has been synthesized in high yield (76%) from 1,5-difluoro-2,4-dinitrobenzene and L-AIa-NH2. This compound contains a reactive fluorine atom which can be used for the reaction with a mixture of L-and D-amino acids. The resulting diastereomers which are ob