2010
DOI: 10.1007/s12221-010-0363-7
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Azocalix[4]pyrrole dyes: Application in dyeing of fibers and their antimicrobial activity

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Cited by 11 publications
(5 citation statements)
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“…Other tetra-azobenzene extended C [4]P have been previously reported, but their photoisomerization behaviors and binding properties were not described. 17,18 Very recently, Wezenberg and co-workers reported the synthesis of a strapped calix [4]pyrrole receptor with a stiff-stilbene unit incorporated in the strap. 19 The switching of the stilbene unit between its Z and E forms significantly reduced the size of the macrocyclic anion binding pocket delimited by the strap.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Other tetra-azobenzene extended C [4]P have been previously reported, but their photoisomerization behaviors and binding properties were not described. 17,18 Very recently, Wezenberg and co-workers reported the synthesis of a strapped calix [4]pyrrole receptor with a stiff-stilbene unit incorporated in the strap. 19 The switching of the stilbene unit between its Z and E forms significantly reduced the size of the macrocyclic anion binding pocket delimited by the strap.…”
Section: Introductionmentioning
confidence: 99%
“…Other tetra-azobenzene extended C[4]P have been previously reported, but their photo-isomerization behaviors and binding properties were not described. 17,18…”
Section: Introductionmentioning
confidence: 99%
“…Calixpyrrole represents a family of supramolecular compounds which are analogues to calixarene. [23] When compared to the chemistry of "traditional" calixarenes, calixpyrroles are particularly attractive compounds due to their unique properties. [24] Numerous receptors can be generated using calix [4]pyrroles due to their huge potential for functionalization.…”
Section: Introductionmentioning
confidence: 99%
“…Tetraazobenzene‐extended calix[4]pyrroles bearing meso ‐methyl substituents were previously reported in literature, however, their molecular recognition and photo‐isomerization properties were not explored , . Herein, we describe an alternative synthetic route for the preparation of tetraazobenzene‐extended calix[4]pyrroles.…”
Section: Introductionmentioning
confidence: 99%
“…[27,28] Tetraazobenzene-extended calix [4]pyrroles bearing mesomethyl substituents were previously reported in literature, however, their molecular recognition and photo-isomerization properties were not explored. [29,30] Herein, we describe an alternative synthetic route for the preparation of tetraazobenzene-extended calix [4]pyrroles. The prepared receptor was isolated as pure tetra-α configurational isomer bearing meso-alkyl substituents functionalized with a terminal ethyl ester.…”
Section: Introductionmentioning
confidence: 99%