Thematische Bibliographien / Double-chain Amphiphiles

Inhaltsverzeichnis

  1. Zeitschriftenartikel
  2. Dissertationen

Auswahl der wissenschaftlichen Literatur zum Thema „Double-chain Amphiphiles“

Autor: Grafiati
Veröffentlicht am 18. Mai 2024
Zuletzt aktualisiert am 31. Juli 2025

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Zeitschriftenartikel zum Thema "Double-chain Amphiphiles"

1

Brun, Alice, та Guita Etemad-Moghadam. "New Double-Chain and Aromatic (α-Hydroxyalkyl)phosphorus Amphiphiles". Synthesis, № 10 (2002): 1385–90. http://dx.doi.org/10.1055/s-2002-33111.

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2

Kimizuka, Nobuo, Takahiro Takasaki, and Toyoki Kunitake. "Polymorphism in Bilayer Membranes of Novel Double-Chain Ammonium Amphiphiles." Chemistry Letters 17, no. 11 (1988): 1911–14. http://dx.doi.org/10.1246/cl.1988.1911.

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3

Koulov, Atanas V., Lauri Vares, Mahim Jain, and Bradley D. Smith. "Cationic triple-chain amphiphiles facilitate vesicle fusion compared to double-chain or single-chain analogues." Biochimica et Biophysica Acta (BBA) - Biomembranes 1564, no. 2 (2002): 459–65. http://dx.doi.org/10.1016/s0005-2736(02)00496-0.

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4

Feast, George C., Thomas Lepitre, Xavier Mulet, et al. "The search for new amphiphiles: synthesis of a modular, high-throughput library." Beilstein Journal of Organic Chemistry 10 (July 10, 2014): 1578–88. http://dx.doi.org/10.3762/bjoc.10.163.

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Amphiphilic compounds are used in a variety of applications due to their lyotropic liquid-crystalline phase formation, however only a limited number of compounds, in a potentially limitless field, are currently in use. A library of organic amphiphilic compounds was synthesised consisting of glucose, galactose, lactose, xylose and mannose head groups and double and triple-chain hydrophobic tails. A modular, high-throughput approach was developed, whereby head and tail components were conjugated using the copper-catalysed azide–alkyne cycloaddition (CuAAC) reaction. The tails were synthesised fr
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5

Cescato, Claudio, Peter Walde, and Pier Luigi Luisi. "Supramolecular Transformations of Vesicles from Amino Acid Based Double Chain Amphiphiles." Langmuir 13, no. 16 (1997): 4480–82. http://dx.doi.org/10.1021/la9701900.

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6

Azum, Naved, Malik Abdul Rub, Anish Khan, Maha M. Alotaibi, Abdullah M. Asiri, and Mohammed M. Rahman. "Mixed Micellization, Thermodynamic and Adsorption Behavior of Tetracaine Hydrochloride in the Presence of Cationic Gemini/Conventional Surfactants." Gels 8, no. 2 (2022): 128. http://dx.doi.org/10.3390/gels8020128.

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In this approach, tensiometry and UV-visible techniques are used to determine the effect of cationic gemini and conventional surfactants on tetracaine hydrochloride (TCH), an anesthetic drug. We have estimated micellar, interfacial, and energetic constraints. To gain a deep understanding of their mixed association behavior, the outputs were examined using different theoretical models. The critical micelle concentration for single and mixed amphiphiles was estimated. The cmc values of mixed amphiphiles were found between the individual amphiphiles due to strong attractive interaction (synergism
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7

Kato, Shinji, and Toyoki Kunitake. "Molecular Design of Black Lipid Membranes (BLM) by Polymerized Double-Chain Ammonium Amphiphiles." Chemistry Letters 20, no. 2 (1991): 261–64. http://dx.doi.org/10.1246/cl.1991.261.

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8

Nakashima, Naotoshi, Norihiro Yamada, and Toyoki Kunitake. "A Fourier transform infrared study of bilayer membranes of double-chain ammonium amphiphiles." Journal of Physical Chemistry 90, no. 15 (1986): 3374–77. http://dx.doi.org/10.1021/j100406a014.

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9

Sugimoto, Masakatsu, Kyoko Shibahara, Kenzi Kuroda, Toshikazu Hirao, Hideo Kurosawa, and Isao Ikeda. "Bilayer Formation and Its Spectral Behavior of Double-Chain Amphiphiles Having Cinnamate Units." Langmuir 12, no. 11 (1996): 2785–90. http://dx.doi.org/10.1021/la9509561.

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10

Masuyama, Araki, Tomoko Kawano, Yun-Peng Zhu, Toshiyuki Kida, and Yohji Nakatsuji. "“Elasticity Index” for the Connecting Groups of Double-Chain Amphiphiles Bearing Two Hydrophilic Groups." Chemistry Letters 22, no. 12 (1993): 2053–56. http://dx.doi.org/10.1246/cl.1993.2053.

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Dissertationen zum Thema "Double-chain Amphiphiles"

1

Paul, Chowdhury Madhurima. "Physicochemical studies on double-chain amphiphiles and their aggregation behavior in different media." Thesis, University of North Bengal, 2018. http://ir.nbu.ac.in/handle/123456789/2692.

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2

Chia-YaoTseng and 曾珈瑤. "Effects of alkyl chain length on the mixed Langmuir monolayer behavior of ion pair amphiphile/cholesterol with double-chained cationic surfactants." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/88948837921588418301.

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碩士<br>國立成功大學<br>化學工程學系碩博士班<br>98<br>In this study, mixed Langmuir monolayer behavior of ion pair amphiphile (IPA), hexadecyltrimethylammonium-dodecylsulfate (HTMA-DS), with various additives was investigated by surface pressure-area and surface potential-area isotherms, relaxation curves, and Brewster angle microscopy (BAM) images. The purpose is to understand the effects of alkyl chain length and molar fraction of dialkyldimethylammonium bromide (DXDAB) on the molecular interaction in the HTMA-DS and HTMA-DS/cholesterol monolayers and on the corresponding mixed monolayer stability. The is
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3

Ting-PinChou and 周廷濱. "Effects of alkyl chain length on the molecular packing characteristic of mixed ion pair amphiphile/double-chained cationic surfactant Langmuir monolayers by infrared spectroscopy." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/99250232111337745944.

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碩士<br>國立成功大學<br>化學工程學系<br>102<br>In this study, infrared reflection-absorption spectroscopy technique is applied to obtain information on the molecular packing properties of mixed IPA/DXDAB monolayers at the air/water interface. The results show that, the HTMA-HS monolayer is stable at the air/water interface while the HTMA-DS monolayer is not. The reason is that the structure of HTMA-DS molecule is asymmetry, and thus the degree of freedom of the carbon tails will be high. For three kinds of DXDAB, the results show that the DODAB monolayer can be stable at the air/water interface and the othe
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