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Collect. Czech. Chem. Commun. 1971, 36, 3608-3620
https://doi.org/10.1135/cccc19713608

Electronic spectra of Schiff's bases of 3-(benzylideneamino)-4-hydroxytoluene and N-(5-methylsalicylidene)aniline types

F. Kristek, J. Klicnar and P. Vetešník

Crossref Cited-by Linking

  • Mandal A, Fitzmaurice D, Waghorne E, Koll A, Filarowski A, Quinn S, Mukherjee S: Proton transfer reaction of a new orthohydroxy Schiff base at room temperature and 77 K. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 2004, 60, 805. <https://doi.org/10.1016/S1386-1425(03)00305-6>
  • Dominiak Paulina M., Grech Eugeniusz, Barr Gordon, Teat Simon, Mallinson Paul, Woźniak Krzysztof: Neutral and Ionic Hydrogen Bonding in Schiff Bases. Chemistry A European J 2003, 9, 963. <https://doi.org/10.1002/chem.200390118>
  • Mandal A., Filarowski A., Glowiaka T., Koll A., Mukherjee S.: Strengthening of the intramolecular hydrogen bond in 7-ethylsalicylidene aniline due to steric repulsion. Journal of Molecular Structure: THEOCHEM 2002, 577, 153. <https://doi.org/10.1016/S0166-1280(01)00658-3>
  • Guha D, Mandal A, Koll A, Filarowski A, Mukherjee S: Proton transfer reaction of a new orthohydroxy Schiff base in protic solvents at room temperature. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 2000, 56, 2669. <https://doi.org/10.1016/S1386-1425(00)00303-6>
  • Maciejewska Dorota, Pawlak Dorota, Koleva Vera: Hydrogen bonding and tautomerism of benzylideneanilines in the solid state. J. Phys. Org. Chem. 1999, 12, 875. <https://doi.org/10.1002/(SICI)1099-1395(199912)12:12<875::AID-POC213>3.0.CO;2-T>
  • Filarowski Aleksander, Głowiaka Tadeusz, Koll Aleksander: Strengthening of the intramolecular O⋯H⋯N hydrogen bonds in Schiff bases as a result of steric repulsion. Journal of Molecular Structure 1999, 484, 75. <https://doi.org/10.1016/S0022-2860(98)00660-7>
  • Filarowski Aleksander, Koll Aleksander, Glowiak Tadeusz, Majewski Eugeniusz, Dziembowska Teresa: Proton transfer reaction in N‐methyl‐2‐hydroxy‐Schiff bases. Ber Bunsenges Phys Chem 1998, 102, 393. <https://doi.org/10.1002/bbpc.19981020317>
  • Salman Salman R., Noor S.: Thermal decomposition of some hydroxy schiff's bases. Thermochimica Acta 1990, 159, 187. <https://doi.org/10.1016/0040-6031(90)80107-A>
  • Kishore K., Sathyanarayana D. N., Bhanu V. A.: 13C and 1H NMR study of N‐5′‐methylsalicylideneanilines. Magnetic Reson in Chemistry 1987, 25, 471. <https://doi.org/10.1002/mrc.1260250602>
  • Mahmoud M.R., Awad A.M., Shaker A.M.: Electronic absorption spectra of some new heterocyclic azomethines derived from nitroso and active methyl compounds. Spectrochimica Acta Part A: Molecular Spectroscopy 1985, 41, 1177. <https://doi.org/10.1016/0584-8539(85)80128-8>
  • Hummel Richard A., Kaufman Donald C.: Ultraviolet spectrometry. Anal. Chem. 1974, 46, 354. <https://doi.org/10.1021/ac60341a029>
  • KRISTEK F., KLICNAR J., VETEANIK P.: ChemInform Abstract: ELEKTRONENSPEKTREN VON 40 SCHIFFSCHEN BASEN DES TYPS 3‐(BENZYLIDEN‐AMINO)‐4‐HYDROXY‐TOLUOL UND N‐(5‐METHYL‐SALICYLIDEN)‐ANILIN. Chemischer Informationsdienst 1972, 3. <https://doi.org/10.1002/chin.197210065>