1978
DOI: 10.1021/ja00485a060
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Chiral aggregation phenomena. 1. Acid dependent chiral recognition in a monolayer

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1978
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Cited by 15 publications
(7 citation statements)
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“…All previous work on acetoxy radical recognized cage decarboxylation (k = 1.6 X 109 s'1)2 as the major pathway, with indications that cage-wall trapping by cyclohexene solvent is the only reaction which competes with decarboxylation; no authenticated noncage reactions were recognized. 3 We observe acetoxy reactions outside the cage which we attribute to ir-acetoxy and we attribute all previous work to -acetoxy. Acetoxy radical is generated in chain reactions of acetyl hypobromite (MeC02Br).…”
supporting
confidence: 67%
“…All previous work on acetoxy radical recognized cage decarboxylation (k = 1.6 X 109 s'1)2 as the major pathway, with indications that cage-wall trapping by cyclohexene solvent is the only reaction which competes with decarboxylation; no authenticated noncage reactions were recognized. 3 We observe acetoxy reactions outside the cage which we attribute to ir-acetoxy and we attribute all previous work to -acetoxy. Acetoxy radical is generated in chain reactions of acetyl hypobromite (MeC02Br).…”
supporting
confidence: 67%
“…11 A variety of artificial host-guest assemblies has been planned to comprehend molecular recognition systems with new properties and functions. Recognition of various aqueous guest molecules, such as nucleic acids, their bases, nucleosides, and nucleotides, [12][13][14][15] barbituric acid and related derivatives, [16][17][18][19] amino acids, saccharides, [20][21][22][23][24][25][26] etc., 27,28 as well as chiral recognition within membrane components [29][30][31][32][33] and/or between amphiphile and aqueous guests [34][35][36][37][38][39][40][41] at the air/water interface have been studied.…”
Section: Introductionmentioning
confidence: 99%
“…The air-water interface has been also used for chiral recognition within membrane components [695][696][697][698][699][700] and/or between amphiphile and aqueous guests [701][702][703][704][705][706][707][708]. Mechanical control of chiral recognition was recently achieved using the novel concept of molecular twisting, as shown in figure 79A, where an octacoordinate sodium complex of a polycholesteryl-substituted cyclen embedded at the air-water interface was used as a molecular host [709].…”
Section: Langmuir-blodgett Filmsmentioning
confidence: 99%