Molecular Insight into Dye-Surfactant Interaction at Premicellar Concentrations : A Combined Two-Photon Absorption and Molecular Dynamics Simulation Study

Both electrostatic and hydrophobic interactions play pivotal roles in ligand-surfactant binding interaction, especially for ionic surfactants. While much studies have been reported in the micellar region, less attention has been paid on such interactions at a low (premicellar) surfactant concentrati...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1999. - 38(2022), 10 vom: 15. März, Seite 3105-3112
1. Verfasser: Islam, Sk Imadul (VerfasserIn)
Weitere Verfasser: Pyne, Partha, Das, Dipak Kumar, Mukherjee, Shounak, Chakrabarty, Suman, Mitra, Rajib Kumar
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2022
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Cations Excipients Micelles Pulmonary Surfactants Surface-Active Agents Carbon 7440-44-0 Cetrimonium Z7FF1XKL7A
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100 1 |a Islam, Sk Imadul  |e verfasserin  |4 aut 
245 1 0 |a Molecular Insight into Dye-Surfactant Interaction at Premicellar Concentrations  |b A Combined Two-Photon Absorption and Molecular Dynamics Simulation Study 
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520 |a Both electrostatic and hydrophobic interactions play pivotal roles in ligand-surfactant binding interaction, especially for ionic surfactants. While much studies have been reported in the micellar region, less attention has been paid on such interactions at a low (premicellar) surfactant concentration. We here study the interaction between the cationic dye rhodamine 6G (R6G) with surfactants of different charge types: anionic SDS, cationic CTAB, and nonionic Tx 100 using absorption and emission spectroscopy. We identify that R6G forms dimeric aggregates at a premicellar concentration of SDS. Formation of aggregates is also confirmed from classical simulation measurements. CTAB and Tx 100 do not form any such aggregate, presumably owing to unfavorable electrostatic interactions. For a molecular-level understanding, we perform two-photon absorption (TPA) spectroscopy for the same systems. TPA allows us to calculate the two-photon absorption cross section and subsequently the change in the dipole moment (Δμ) between ground and excited states of the dye. We calculate the Δμ and observe that it passes through a maximum at a surfactant concentration half of the critical micelle concentration of SDS. This observation imparts support to earlier quantum mechanical calculation, which infers deviation from the parallel orientation of the dye during surfactant-induced aggregation. We extended our measurements and varied the carbon chain length of the anionic surfactant, and we found that all of them exhibit a maximum in Δμ, while their relative magnitude is dependent on the surfactant carbon chain length 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
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650 7 |a Micelles  |2 NLM 
650 7 |a Pulmonary Surfactants  |2 NLM 
650 7 |a Surface-Active Agents  |2 NLM 
650 7 |a Carbon  |2 NLM 
650 7 |a 7440-44-0  |2 NLM 
650 7 |a Cetrimonium  |2 NLM 
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700 1 |a Pyne, Partha  |e verfasserin  |4 aut 
700 1 |a Das, Dipak Kumar  |e verfasserin  |4 aut 
700 1 |a Mukherjee, Shounak  |e verfasserin  |4 aut 
700 1 |a Chakrabarty, Suman  |e verfasserin  |4 aut 
700 1 |a Mitra, Rajib Kumar  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Langmuir : the ACS journal of surfaces and colloids  |d 1999  |g 38(2022), 10 vom: 15. März, Seite 3105-3112  |w (DE-627)NLM098181009  |x 1520-5827  |7 nnns 
773 1 8 |g volume:38  |g year:2022  |g number:10  |g day:15  |g month:03  |g pages:3105-3112 
856 4 0 |u http://dx.doi.org/10.1021/acs.langmuir.1c02999  |3 Volltext 
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