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<Articles><Article><Journal><PublisherName></PublisherName><JournalTitle>DARU Journal of Pharmaceutical Sciences</JournalTitle><Volume>12</Volume><Issue>2</Issue></Journal><ArticleTitle>"Synthsis of 6-(2-naphthyl)-2,3-dihydro-as-triazine-3-thione as a Sensitive Reagent for the Spectrophotometric determination of Cu (II) "</ArticleTitle><FirstPage>76</FirstPage><LastPage>80</LastPage><AuthorList><Author><FirstName></FirstName><LastName>Fazel Shamsa</LastName></Author><Author><FirstName></FirstName><LastName>Maliheh Barazandeh-Tehrani</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2015</Year><Month>10</Month><Day>06</Day></PubDate></History><Abstract>A Spectrophotometric method for determination of Cu (II) based on the complex formation with a new reagent 6-(2-naphthyl)-2,3-dihydro-as-triazine-3-thione(NDTT) is described. NDTT was synthesized based on the knowledge available for the preparation of 6-phenyl-2,3-dihydro-as-triazine-3-thione (PDTT). Reaction of 2-acetylnaphthalene 1 with amyl nitrite gave 2-naphthylglyoxal aldoxime 2, which upon reaction with thiosemicarbazide yielded 6-(2-naphthyl)-2,3-dihydro-as-triazine-3-thione (NDTT) 3.
NDTT produces a red complex with copper which is easily extractable with chloroform at pH&gt;8 while the reagent is not extracted under these conditions. The absorption of the complex in the UV region (313 nm) is about 7 times greater than in the visible region (508 nm). The mole ratio of the complex which is formed between Cu (II) and NDTT is 2:3, which was calculated by both the mole ratio and the continuous variation methods. The absorbance of the complex obeys Beer’s law in the concentration range of 0.08-2 µg Cu(II)/ml chloroform with r = 0.998 and detection limit of 13 ng/ml. This procedure can be carried out in the presence of many cations and anions in the presence or absence of the masking agents.</Abstract><web_url>https://daru.tums.ac.ir/index.php/daru/article/view/205</web_url><pdf_url>https://daru.tums.ac.ir/index.php/daru/article/download/205/205</pdf_url></Article></Articles>
