2015
DOI: 10.1016/j.dyepig.2015.04.014
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Synthesis and X-ray analysis of a perfluoroalkyl-substituted azobenzene dye

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Cited by 5 publications
(2 citation statements)
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“…Azobenzene and its derivatives comprise a dominant class of synthetic colorants that demonstrate the advantages of bright colors, good stability, low flammability, and reversible photoisomerization [56,57]. Aromatic esters have been reported to display electrochromic properties through the formation of anionic radicals via electrochemical reduction [58][59][60][61][62].…”
Section: Introductionmentioning
confidence: 99%
“…Azobenzene and its derivatives comprise a dominant class of synthetic colorants that demonstrate the advantages of bright colors, good stability, low flammability, and reversible photoisomerization [56,57]. Aromatic esters have been reported to display electrochromic properties through the formation of anionic radicals via electrochemical reduction [58][59][60][61][62].…”
Section: Introductionmentioning
confidence: 99%
“…[18][19][20] In this way,t he effectiveness of the denitrification-diazotization step can be evaluated in combination with as ubsequent azo coupling reaction, at which this two-step sequence is also of fundamental importance for the multi-ton scale productiono f ab road range of azo compounds used as dyes for textiles and many other purposes. [21,22] From ap harmaceutical point of view,t reatments with balsalazide (1), olsalazine (2)a nd sulfasalazine (3)r equires ignificant amountso ft hese compounds reaching maximum doses in the range of 2-6 grams/day for acute illnesses. [23] Through cleav-age in the intestine, all three compounds can act as pro-drugs for 5-aminosalicylic acid (5-ASA, mesalazine), which is active against inflammatory bowel disease including ulcerative colitis and Crohn's disease.…”
mentioning
confidence: 99%