Piezoluminescence at the Air−Water Interface through Dynamic Molecular Recognition Driven by Lateral Pressure Application
- 24 December 2004
- journal article
- research article
- Published by American Chemical Society (ACS) in Langmuir
- Vol. 21 (3), 976-981
- https://doi.org/10.1021/la0477845
Abstract
The steroid cyclophanes with a cyclic core consisting of a 1,6,20,25-tetraaza[6.1.6.1]paracyclophane connected to four steroid moieties (cholic acid or cholanic acid) through a flexible l-lysine spacer were spread on water as Langmuir monolayers. The π−A isotherm of the cholic-type steroid cyclophane includes a transition to the condensed phase with a limiting area of ∼2 nm2. This value is close to the cross-sectional area of the steroid cyclophane with a standing-up conformation of the cholic acid moieties, strongly suggesting that the cavity converts from a two-dimensional cavity to a three-dimensional cavity upon compressing the monolayer. Surface-reflective fluorescence spectroscopy of the monolayer using an aqueous fluorescent probe (6-(p-toluidino)naphthalene-2-sulfonate (TNS)) showed an abrupt increase in the TNS fluorescence intensity at a molecular area of 2 nm2. Efficient binding of the guest probe would occur upon the completion of the three-dimensional cavity. Repeated compression and expansion induces periodic changes in the fluorescence intensity. This indicates a piezoluminescence effect through the catch and release of the TNS guest upon dynamic cavity formation. Analyses of the binding behavior of TNS to the steroid cyclophane resulted in binding constants in the range of ∼(5−9) × 104 M-1 which are similar to that observed in lipid bilayer media (K = 5.1 × 104 M-1). The fluorescence intensity within the condensed phase was significantly increased with increasing pressure, suggesting that suppression of the molecular motion of the bound TNS may retard the nonemission process. Similar monolayer experiments were carried out with the monolayer of the cholanic-type steroid cyclophane that cannot form an open conformation on water. Both the phase transition in the π−A isotherm and the change in the fluorescence intensity were negligible, confirming that the dynamic characteristic of the cavity is indispensable for the efficient pressure-induced binding of the guest and the consequent luminescence.Keywords
This publication has 53 references indexed in Scilit:
- Fluorophore Appended Saccharide Cyclophane: Self-Association, Fluorescent Properties, Heterodimers with Cyclodextrins, and Cross-Linking Behavior with Peanut Agglutinin of Dansyl-Modified Saccharide CyclophaneThe Journal of Organic Chemistry, 2004
- Effect of pressure on the critical micelle concentration of neutral surfactant using fluorescence probe methodJournal of Photochemistry and Photobiology A: Chemistry, 1999
- Molecular Recognition-Induced Function and Competitive Replacement by Hydrogen-Bonding Interactions: Amphiphilic Barbituric Acid Derivatives, 2,4,6-Triaminopyrimidine, and Related Structures at the Air−Water InterfaceLangmuir, 1998
- Surface Chemical and Morphological Study on Monolayers of Cholesterol, Cholestanol, and Their Derivatives Conjugated with Amino AcidLangmuir, 1997
- Molecular Recognition of Organized Assemblies via hydrogen bonding in aqueous mediaAdvanced Materials, 1997
- Circular Dichroism of an Aromatic Guest Induced by a Chiral Steroid Cyclophane in Aqueous Solution and Synthetic Bilayer MembraneChemistry Letters, 1996
- How to Transfer Monolayer Maintaining Its Crystallographic Structure on the Water Surface by the Horizontal Drawing-up MethodChemistry Letters, 1994
- Steroid cyclophanes as artificial receptors embedded in synthetic bilayer membranes: Aggregation behavior and molecular recognitionRecueil des Travaux Chimiques des Pays-Bas, 1994
- Design and Syntheses of Paracyclophanes Having Charged Side Chains That Are Soluble in Neutral Aqueous SolutionHETEROCYCLES, 1981
- A Spectrophotometric Investigation of the Interaction of Iodine with Aromatic HydrocarbonsJournal of the American Chemical Society, 1949