Chemical and Photochemical Studies on 1,8-Diaminonaphthalene | ||||
Egyptian Journal of Chemistry | ||||
Article 47, Volume 65, Issue 3, March 2022, Page 501-506 PDF (350.09 K) | ||||
Document Type: Original Article | ||||
DOI: 10.21608/ejchem.2021.94861.4462 | ||||
View on SCiNiTO | ||||
Authors | ||||
asma Mahran1; Sherif Ragab 2; Dalia Othman1 | ||||
1Photochemistry Department, Chemical Industries Research Division, National Research Centre (NRC), El behouth Street, Dokki, Giza, 12622, Egypt | ||||
2National Research Centre | ||||
Abstract | ||||
A novel series of naphthodiazepines 4a-e, 6 were synthesized through the reaction of 1,8-diaminonaphthalene 1 with either hydrazonoyl chlorides 2a-e, or bis-hydrazonoyl chloride 5, respectively. Moreover, new derivatives of thiazinoperimidine 9, triazoloperimidine 13 , and thiazoloperimidines 14,17 were produced upon the interaction of 1H-perimidine-2-thiol 7 with the reagents; epichlorohydrin, hydrazonoyl chloride 10, bis-hydrazonoyl chloride 5, and α-chloroacetoacetanilide 15, respectively. Additionally, the irradiation of 1,8-diaminonaphthalene 1 was accomplished at λ > 313 nm using a high-pressure mercury lamp in the presence of oxygen. All the products were characterized using spectroscopic and analytical techniques | ||||
Keywords | ||||
naphthodiazepine; bis-hydrazonoyl; perimidine; irradiation | ||||
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