{"title":"盐酸1-萘胺席夫碱的合成与表征，叙利亚:Homs","authors":"Rawand Alsabra","doi":"10.7176/cmr/13-3-02","DOIUrl":null,"url":null,"abstract":"The three Schiff bases namely NPNA (L 1 ): N-[(E)-Pheny lmethylene]Naphthalene-1-Amine, newly NNNA (L 2 ): N-[(E)-1-Naphthylmethylene]Naphthalene-1-Amine and NFNA (L 3 ): N-[(E)-2-Furylmethylene] Naphthalene-1-Amine have been synthesized in equimolar reaction of 1-Naphthylamine hydrochloride with or naphthalene-1-carbaldehyde or 2-furfuraldehyde in the presence of acetic acid glacial. The characterization of Schiff bases was done by 1 HNMR, UV–VIS, IR, spectral studies and analytical data.","PeriodicalId":9724,"journal":{"name":"chemistry and materials research","volume":"28 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis and Characterization of Schiff Bases Derived from 1-Naphthylamine Hydrochloride, Syria: Homs\",\"authors\":\"Rawand Alsabra\",\"doi\":\"10.7176/cmr/13-3-02\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The three Schiff bases namely NPNA (L 1 ): N-[(E)-Pheny lmethylene]Naphthalene-1-Amine, newly NNNA (L 2 ): N-[(E)-1-Naphthylmethylene]Naphthalene-1-Amine and NFNA (L 3 ): N-[(E)-2-Furylmethylene] Naphthalene-1-Amine have been synthesized in equimolar reaction of 1-Naphthylamine hydrochloride with or naphthalene-1-carbaldehyde or 2-furfuraldehyde in the presence of acetic acid glacial. The characterization of Schiff bases was done by 1 HNMR, UV–VIS, IR, spectral studies and analytical data.\",\"PeriodicalId\":9724,\"journal\":{\"name\":\"chemistry and materials research\",\"volume\":\"28 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"chemistry and materials research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.7176/cmr/13-3-02\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"chemistry and materials research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7176/cmr/13-3-02","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis and Characterization of Schiff Bases Derived from 1-Naphthylamine Hydrochloride, Syria: Homs
The three Schiff bases namely NPNA (L 1 ): N-[(E)-Pheny lmethylene]Naphthalene-1-Amine, newly NNNA (L 2 ): N-[(E)-1-Naphthylmethylene]Naphthalene-1-Amine and NFNA (L 3 ): N-[(E)-2-Furylmethylene] Naphthalene-1-Amine have been synthesized in equimolar reaction of 1-Naphthylamine hydrochloride with or naphthalene-1-carbaldehyde or 2-furfuraldehyde in the presence of acetic acid glacial. The characterization of Schiff bases was done by 1 HNMR, UV–VIS, IR, spectral studies and analytical data.
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