2009
DOI: 10.1039/b813498g
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Endowing catanionic surfactant vesicles with dual responsive abilities via a noncovalent strategy: introduction of a responser, sodium cholate

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Cited by 52 publications
(40 citation statements)
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(50 reference statements)
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“…The vector approach is, however, by no means limited to directed assembly. It is possible to mix a trace amount of carefully designed pin molecules with a large amount of dummy molecules so that molecular assemblies can be massively produced and be switched between micelles, vesicles and tubes upon simple clicks 28 . Second, chemical fixation of the vector structure is envisioned to be feasible given a number of well-established methods such as sintering, polymer grafting and cross-linking, and capillary condensation 29 30 31 .…”
Section: Discussionmentioning
confidence: 99%
“…The vector approach is, however, by no means limited to directed assembly. It is possible to mix a trace amount of carefully designed pin molecules with a large amount of dummy molecules so that molecular assemblies can be massively produced and be switched between micelles, vesicles and tubes upon simple clicks 28 . Second, chemical fixation of the vector structure is envisioned to be feasible given a number of well-established methods such as sintering, polymer grafting and cross-linking, and capillary condensation 29 30 31 .…”
Section: Discussionmentioning
confidence: 99%
“…Upon irradiation by UV light, OMCA undergoes a photo-isomerization from cis to trans, altering molecular packing at the interface, thus drastically reducing micellar length and resulting in a viscosity decrease by four orders of magnitude. The strategy proposed by Jiang et al [27] was successfully extended to other surfactants mixtures. It has the obvious advantage of sidestepping difficult synthesis, while the nature of the responser can easily be extended to a range of molecules, as long as they present some hydrophobicity, so that they can spontaneously be incorporated into micellar aggregates: hydrotropes, dyes, light-responsive cinnamic acid, redox-responsive ferrocene carboxylic acid, and pH-responsive malachite green.…”
Section: Multi-stimuli-responsive Wlmsmentioning
confidence: 97%
“…Also relevant to the field of WLMs, because it suggests potential non-covalent routes to impart them, multi-stimuli responsiveness is the work reported by Huang and co-workers [27] on surfactant aggregates. Multi-stimuli responsiveness was imparted to otherwise responsiveness catanionic (mixtures of cationic and anionic) surfactants by the simple addition of a "responser" (a multi-stimuli-responsive molecule) in sodium cholate (SC), which has three temperature-responsive hydroxyl groups, a pH-responsive carboxylate group and a hydrophobic steroid skeleton.…”
Section: Multi-stimuli-responsive Wlmsmentioning
confidence: 97%
“…Except for temperaturecontrolled or salt-induced vesicle-to-micelle transitions in those asymmetric systems explained by ion-pair solubility mismatch, 11,32,54 the transition from vesicles to micelles found in many mixtures of cationic-anionic surfactants with similar chain length inducing by temperature and bio amphiphiles could be well explained by the packing parameter, involving the factors such as the volume of hydrophobic chains, 55 the charge density, 56 and the average headgroup area. 57 As an exception, for the symmetric mixtures of sodium dodecylsulfate (SDS) and dodecyltrimethylammonium bromide (DTAB) whose compositions are far from equimolarity, the vesicle-to-micelle transition by adding 0.1 M NaBr can be rationalized as a consequence of the transition of free monomers into the aggregates as the chemical potential of the surfactant in excess is lowered upon addition of salt. 12 The addition of salts has multiple effects on a surfactant solution, such as a ''salting-out'' effect, and ''screening'' effect on either inter-aggregate or intra-aggregate electrostatic repulsions due to the like-charged headgroups of surfactants.…”
Section: Mechanism From Packing Parametermentioning
confidence: 99%