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Journal articles on the topic 'Double-chain Amphiphiles'

Author: Grafiati

Published: 18 May 2024

Last updated: 19 July 2025

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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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11

Kunitake, Toyoki, Naotoshi Nakashima, and Masashi Kunitake. "Polymerization and membrane characteristics of aqueous bilayers of glutamate-based double-chain ammonium amphiphiles." Macromolecules 22, no. 9 (1989): 3544–50. http://dx.doi.org/10.1021/ma00199a008.

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12

Leventis, Rania, Thomas Diacovo, and John R. Silvius. "pH-dependent stability and fusion of liposomes combining protonatable double-chain amphiphiles with phosphatidylethanolamine." Biochemistry 26, no. 12 (1987): 3267–76. http://dx.doi.org/10.1021/bi00386a005.

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13

Sumida, Yasushi, Araki Masuyama, Toshihiro Oki, et al. "Pressure−Area Isotherms for Double-Chain Amphiphiles Bearing Two Hydroxyl Groups Derived from Diepoxides." Langmuir 12, no. 16 (1996): 3986–90. http://dx.doi.org/10.1021/la960268x.

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14

Zhou, Tianhua, Jianxi Zhao, and Yi You. "Effect of the Interionic Distance on the Interfacial Behavior of Double-Chain Zwitterionic Amphiphiles." Journal of Dispersion Science and Technology 30, no. 8 (2009): 1135–41. http://dx.doi.org/10.1080/01932690802701556.

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15

Silvius, John R. "Anomalous mixing of zwitterionic and anionic phospholipids with double-chain cationic amphiphiles in lipid bilayers." Biochimica et Biophysica Acta (BBA) - Biomembranes 1070, no. 1 (1991): 51–59. http://dx.doi.org/10.1016/0005-2736(91)90145-x.

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16

Tojinbara, Toru, Masaaki Akamatsu, Kenichi Sakai, and Hideki Sakai. "Oil-in-Water Emulsions Stabilized by Acylglutamic Acid–Alkylamine Complexes as Noncovalent-Type Double-Chain Amphiphiles." Langmuir 34, no. 1 (2017): 268–72. http://dx.doi.org/10.1021/acs.langmuir.7b03468.

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17

Clary, Laurence, Jacques Greiner, Catherine Santaella та Pierre Vierling. "synthesis of single- and double-chain fluorocarbon and hydrocarbon β-linked galactose amphiphiles derived from serine". Tetrahedron Letters 36, № 4 (1995): 539–42. http://dx.doi.org/10.1016/0040-4039(94)02335-9.

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18

Jung, Jong Hwa, Youngkyu Do, Young-A. Lee, and Toshimi Shimizu. "Self-Assembling Structures of Long-Chain Sugar-Based Amphiphiles Influenced by the Introduction of Double Bonds." Chemistry - A European Journal 11, no. 19 (2005): 5538–44. http://dx.doi.org/10.1002/chem.200401288.

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19

Wakayama, Yutaka, and Toyoki Kunitake. "Direct Observation of Ordered Bilayers in Cast Films of Double-Chain Ammonium Amphiphiles by Transmission Electron Microscopy." Chemistry Letters 22, no. 8 (1993): 1425–28. http://dx.doi.org/10.1246/cl.1993.1425.

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20

Song, Yao, Jiani Gong, Xiaoting Xu, et al. "Specific ion effects on the self-assembly and interfacial properties of double- and single-chain cationic amphiphiles." Journal of Molecular Liquids 414 (November 2024): 126290. http://dx.doi.org/10.1016/j.molliq.2024.126290.

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21

Faroux-Corlay, Barbara, Laurence Clary, Catherine Gadras, et al. "Synthesis of single- and double-chain fluorocarbon and hydrocarbon galactosyl amphiphiles and their anti-HIV-1 activity." Carbohydrate Research 327, no. 3 (2000): 223–60. http://dx.doi.org/10.1016/s0008-6215(00)00055-0.

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22

Nakashima, Naotoshi, Reiko Ando, and Toyoki Kunitake. "Fluorescence Behavior and Energy Transfer of Cyanine Dyes Bound to Bilayer Membranes of Double-Chain Ammonium Amphiphiles." Bulletin of the Chemical Society of Japan 60, no. 6 (1987): 1967–73. http://dx.doi.org/10.1246/bcsj.60.1967.

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23

Feast, George C., Thomas Lepitre, Nhiem Tran, et al. "Inverse hexagonal and cubic micellar lyotropic liquid crystalline phase behaviour of novel double chain sugar-based amphiphiles." Colloids and Surfaces B: Biointerfaces 151 (March 2017): 34–38. http://dx.doi.org/10.1016/j.colsurfb.2016.12.004.

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24

Jouani, M. A., S. Szönyi, H. Trabelsi, S. Y. Dieng, A. Cambon, and H. J. Watzke. "Synthesis and aggregation properties of new fluorine-containing double-chain amphiphiles derived from di- and tri-substituted ureas." Supramolecular Science 2, no. 2 (1995): 117–23. http://dx.doi.org/10.1016/0968-5677(96)89076-6.

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25

CLARY, L., J. GREINER, C. SANTAELLA, and P. VIERLING. "ChemInform Abstract: Synthesis of Single- and Double-Chain Fluorocarbon and Hydrocarbon . beta.-Linked Galactose Amphiphiles Derived from Serine." ChemInform 26, no. 22 (2010): no. http://dx.doi.org/10.1002/chin.199522269.

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26

Hong, Bing, Jonathan Lai, Loïc Leclercq, et al. "Binary and Ternary Phase Behaviors of Short Double-Chain Quaternary Ammonium Amphiphiles: Surface Tension, Polarized Optical Microscopy, and SAXS Investigations." Journal of Physical Chemistry B 117, no. 47 (2013): 14732–42. http://dx.doi.org/10.1021/jp406062b.

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27

Kato, Shinji, and Toyoki Kunitake. "Aqueous Bilayers of Glutamate-Based Double-Chain Ammonium Amphiphiles II. Improvement of Polymerization and Membrane Characteristics by Ether-Linked Alkyl Tails." Polymer Journal 23, no. 2 (1991): 135–46. http://dx.doi.org/10.1295/polymj.23.135.

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28

Clary, Laurence, Catherine Gadras, Jacques Greiner, et al. "Phase behavior of fluorocarbon and hydrocarbon double-chain hydroxylated and galactosylated amphiphiles and bolaamphiphiles. Long-term shelf-stability of their liposomes." Chemistry and Physics of Lipids 99, no. 2 (1999): 125–37. http://dx.doi.org/10.1016/s0009-3084(99)00032-8.

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29

Ishikawa, Yuichi, Hiroaki Kuwahara, and Toyoki Kunitake. "Self-assembly of bilayers from double-chain fluorocarbon amphiphiles in aprotic organic solvents: thermodynamic origin and generalization of the bilayer assembly." Journal of the American Chemical Society 116, no. 13 (1994): 5579–91. http://dx.doi.org/10.1021/ja00092a008.

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30

Liang, Kang-Ning, and Yong-Zheng Hui. "Investigation in monolayers of double-chain fluorocarbon amphiphiles Effect of headgroups on molecular packing and interaction between hydrocarbon and fluorocarbon monolayers." Chinese Journal of Chemistry 10, no. 6 (2010): 481–86. http://dx.doi.org/10.1002/cjoc.19920100601.

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31

Pinazo, Aurora, Ramon Pons, Ana Marqués, Maribel Farfan, Anderson da Silva, and Lourdes Perez. "Biocompatible Catanionic Vesicles from Arginine-Based Surfactants: A New Strategy to Tune the Antimicrobial Activity and Cytotoxicity of Vesicular Systems." Pharmaceutics 12, no. 9 (2020): 857. http://dx.doi.org/10.3390/pharmaceutics12090857.

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Their stability and low cost make catanionic vesicles suitable for application as drug delivery systems. In this work we prepared catanionic vesicles using biocompatible surfactants: two cationic arginine-based surfactants (the monocatenary Nα-lauroyl-arginine methyl ester—LAM and the gemini Nα,Nϖ-bis(Nα-lauroylarginine) α, ϖ-propylendiamide—C3(CA)2) and three anionic amphiphiles (the single chain sodium dodecanoate, sodium myristate, and the double chain 8-SH). The critical aggregation concentration, colloidal stability, size, and charge density of these systems were comprehensively studied f

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32

Enjalbert, D., C. Bassilana, and S. Szonyi. "Synthesis of new double-chain cationic and amphoteric F-alkylated amphiphiles derived from N-alkyl N-methyl N-[2-(F-alkyl)ethyl] amines." Tenside Surfactants Detergents 35, no. 4 (1998): 248–52. http://dx.doi.org/10.1515/tsd-1998-350404.

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33

Ariga, Katsuhiko, and Yoshio Okahata. "Permeability controllable membranes. 11. Polymerized monolayers of single-, double-, and triple-chain silane amphiphiles and permeation control through the monolayer-immobilized porous glass plate in an aqueous solution." Journal of the American Chemical Society 111, no. 15 (1989): 5618–22. http://dx.doi.org/10.1021/ja00197a018.

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34

Guo Bin, Luo, Liu Ting-Ting, Yu An-Chi, et al. "Self-Organiztion of a Double Chain Amphiphile DDPA Investigated by AFM." Acta Physico-Chimica Sinica 15, no. 05 (1999): 385–89. http://dx.doi.org/10.3866/pku.whxb19990501.

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35

Luo, Guobin, Tingting Liu, Liming Ying, et al. "Aggregation and Self-Organization of a Chromophore-Labeled Double-Chain Amphiphile." Langmuir 16, no. 8 (2000): 3651–59. http://dx.doi.org/10.1021/la991226m.

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36

MORISHIMA, Yotaro, Michiko SEKI, Shigeki NOMURA, and Mikiharu KAMACHI. "Novel Coulombic Complexes of Amphiphilic Polyelectrolytes and Double-chain Surfactants." Proceedings of the Japan Academy. Ser. B: Physical and Biological Sciences 69, no. 4 (1993): 83–88. http://dx.doi.org/10.2183/pjab.69.83.

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37

Pector, Véronique, Jacques Caspers, Sunanda Banerjee, et al. "Physico-chemical characterization of a double long-chain cationic amphiphile (Vectamidine) by microelectrophoresis." Biochimica et Biophysica Acta (BBA) - Biomembranes 1372, no. 2 (1998): 339–46. http://dx.doi.org/10.1016/s0005-2736(98)00074-1.

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38

Shimomura, Masatsugu, Koichi Fujii, Peter Karg, et al. "Homogeneous Langmuir-Blodgett Film of Double-Chain Ammonium Amphiphile Complexed with Anionic Polymer." Japanese Journal of Applied Physics 27, Part 2, No. 9 (1988): L1761—L1763. http://dx.doi.org/10.1143/jjap.27.l1761.

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39

Uota, Masafumi, Mitsunori Yada, Masako Kuroki, Masato Machida, and Tsuyoshi Kijima. "Carbons from furan-polymers prepared in the presence of a double-chain amphiphile." Carbon 42, no. 11 (2004): 2207–13. http://dx.doi.org/10.1016/j.carbon.2004.04.033.

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40

Seki, Michiko, Yotaro Morishima, and Mikiharu Kamachi. "Characterization of the complexes of amphiphilic polyanions and double-chain cationic surfactants." Macromolecules 25, no. 24 (1992): 6540–46. http://dx.doi.org/10.1021/ma00050a024.

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41

Greiner, J., E. Myrtil, E. Dere, et al. "Double-chain amphiphilic telomers derived from tris-(hydroxymethyl)amidomethane for biomedical applications." Journal of Fluorine Chemistry 58, no. 2-3 (1992): 195. http://dx.doi.org/10.1016/s0022-1139(00)80645-4.

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42

Gonçalves, Rui A., Yeng-Ming Lam, and Björn Lindman. "Double-Chain Cationic Surfactants: Swelling, Structure, Phase Transitions and Additive Effects." Molecules 26, no. 13 (2021): 3946. http://dx.doi.org/10.3390/molecules26133946.

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Double-chain amphiphilic compounds, including surfactants and lipids, have broad significance in applications like personal care and biology. A study on the phase structures and their transitions focusing on dioctadecyldimethylammonium chloride (DODAC), used inter alia in hair conditioners, is presented. The phase behaviour is dominated by two bilayer lamellar phases, Lβ and Lα, with “solid” and “melted” alkyl chains, respectively. In particular, the study is focused on the effect of additives of different polarity on the phase transitions and structures. The main techniques used for investiga

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43

Hägerstrand, Henry, Malgorzata Danieluk, Malgorzata Bobrowska-Hägerstrand, et al. "Liposomes composed of a double-chain cationic amphiphile (Vectamidine) induce their own encapsulation into human erythrocytes." Biochimica et Biophysica Acta (BBA) - Biomembranes 1421, no. 1 (1999): 125–30. http://dx.doi.org/10.1016/s0005-2736(99)00116-9.

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44

Abosheasha, Mohammed A., Toru Itagaki, Yoshihiro Ito, and Motoki Ueda. "Tubular Assembly Formation Induced by Leucine Alignment along the Hydrophobic Helix of Amphiphilic Polypeptides." International Journal of Molecular Sciences 22, no. 21 (2021): 12075. http://dx.doi.org/10.3390/ijms222112075.

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The introduction of α-helical structure with a specific helix–helix interaction into an amphipathic molecule enables the determination of the molecular packing in the assembly and the morphological control of peptide assemblies. We previously reported that the amphiphilic polypeptide SL12 with a polysarcosine (PSar) hydrophilic chain and hydrophobic α-helix (l-Leu-Aib)6 involving the LxxxLxxxL sequence, which induces homo-dimerization due to the concave–convex interaction, formed a nanotube with a uniform 80 nm diameter. In this study, we investigated the importance of the LxxxLxxxL sequence f

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45

Zhai, Jiali, Randy Suryadinata, Bao Luan, et al. "Amphiphilic brush polymers produced using the RAFT polymerisation method stabilise and reduce the cell cytotoxicity of lipid lyotropic liquid crystalline nanoparticles." Faraday Discussions 191 (2016): 545–63. http://dx.doi.org/10.1039/c6fd00039h.

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Self-assembled lipid lyotropic liquid crystalline nanoparticles such as hexosomes and cubosomes contain internal anisotropic and isotropic nanostructures, respectively. Despite the remarkable potential of such nanoparticles in various biomedical applications, the stabilisers used in formulating the nanoparticles are often limited to commercially available polymers such as the Pluronic block copolymers. This study explored the potential of using Reversible Addition-Fragmentation chain Transfer (RAFT) technology to design amphiphilic brush-type polymers for the purpose of stabilising phytantriol

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46

Higashi, Nobuyuki, Toyoki Kunitake, and Tisato Kajiyama. "Efficient Oxygen Enrichment by a Langmuir-Blodgett Film of the Polyion Complex of a Double-Chain Fluorocarbon Amphiphile." Polymer Journal 19, no. 2 (1987): 289–91. http://dx.doi.org/10.1295/polymj.19.289.

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47

Lee, Jung, and Chien-Hsiang Chang. "DNA association-enhanced physical stability of catanionic vesicles composed of ion pair amphiphile with double-chain cationic surfactant." Colloids and Surfaces B: Biointerfaces 121 (September 2014): 171–77. http://dx.doi.org/10.1016/j.colsurfb.2014.06.005.

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48

Hammerschick, Tim, and Walter Vetter. "Profiling and Isolation of Ten Rare Branched-Chain Alkylresorcinols in Quinoa." Molecules 28, no. 13 (2023): 5220. http://dx.doi.org/10.3390/molecules28135220.

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Alkylresorcinols (∑ARs) are bioactive lipid compounds predominantly found in cereals. These amphiphilic compounds exist in a high structural diversity and can be divided into two main groups, i.e., 5-alkylresorcinols (ARs) and 2-methyl-5-alkylresorcinols (mARs). The pseudocereal quinoa has a very unique AR profile, consisting not only of straight-chain alkyl chains but also iso- and anteiso-branched isomers. Here, we describe a method for the isolation of such methyl-branched ARs and mARs from quinoa. The enrichment of the ∑AR fraction from the lipid extracts by centrifugal partition chromatog

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49

Kocsisné Pfeifer, Éva, János Mink, István Gábor Gyurika, and Judit Telegdi. "Effect of Heat Treatment on the Structure of Self-Assembled Undecenyl Phosphonic Acid Layers Developed on Different Stainless Steel Surfaces." Hungarian Journal of Industry and Chemistry 51, no. 2 (2023): 7–14. http://dx.doi.org/10.33927/hjic-2023-12.

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Deterioration caused by corrosion is well known, which can destroy metallic and non-metallic materials alike. Dissolved inhibitors of bionic micro- and nanocoatings can decrease the degree of undesirable corrosion in various ways. In this paper, a self-assembled molecular layer formed from undecenyl phosphonic acid developed on two different steel surfaces was the subject of our experiments. The influence of the metal composition, layer-forming conditions and post-heat treatment was documented by wettability measurements as well as surface roughness parameters; the change in surface morphology

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50

Gerardos, Angelica Maria, and Stergios Pispas. "Double Hydrophilic Hyperbranched Copolymer-Based Lipomer Nanoparticles: Copolymer Synthesis and Co-Assembly Studies." Polymers 16, no. 22 (2024): 3129. http://dx.doi.org/10.3390/polym16223129.

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Double hydrophilic, random, hyperbranched copolymers were synthesized via reversible addition–fragmentation chain transfer (RAFT) polymerization of oligo(ethylene glycol) methyl ether methacrylate (OEGMA) and 2-(dimethylamino)ethyl methacrylate (DMAEMA) utilizing ethylene glycol dimethacrylate (EGDMA) as the branching agent. The resulting copolymers were characterized in terms of their molecular weight and dispersity using size exclusion chromatography (SEC), and their chemical structure was confirmed using FT-IR and 1H-NMR spectroscopy techniques. The choice of the two hydrophilic blocks and

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