2011
DOI: 10.1016/j.tetlet.2010.12.107
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Improved functionality and control in the isomerization of a calix[4]arene-capped azobenzene

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Cited by 16 publications
(6 citation statements)
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“…Photoactive azo residue was also used for joining two molecules of calix[4]arenes to form dimeric structures (Fig. 72 ) [ 218 ]. Azo linked calix[4]arene 171 exists in a locked trans form [ 219 ].…”
Section: Calixarenes With Azo Groupmentioning
confidence: 99%
See 1 more Smart Citation
“…Photoactive azo residue was also used for joining two molecules of calix[4]arenes to form dimeric structures (Fig. 72 ) [ 218 ]. Azo linked calix[4]arene 171 exists in a locked trans form [ 219 ].…”
Section: Calixarenes With Azo Groupmentioning
confidence: 99%
“…
Fig. 72 Dimeric azocalix[4]arenes: 171 —not isomerisable, 172 —undergoing reversible trans – cis isomerization [ 218 ]
…”
Section: Calixarenes With Azo Groupmentioning
confidence: 99%
“…Since the investigation of calixarenes dealing with their syntheses, reactivity and a large variety of applications is very intense, [55][56][57][58][59][60][61][62][63][64][65][66][67][68][69][70] only selected examples of considered compounds are described in this review.…”
Section: Resultsmentioning
confidence: 99%
“…It contains polar NH group required for anion binding and is able to reverse E/Z-isomerization under light influence. [28][29][30] Introduction of ester fragment in a macrocycle structure is necessary for realization of the template effect of alkali metal cations at the synthesis of thiacalix [4]arene stereoisomers. Besides, it is known that introduction of an ethoxycarbonyl fragment in the lower rim of a macrocycle significantly influences on the complex formation with anions.…”
Section: Synthesis Of Thiacalix[4]arenesmentioning
confidence: 99%