Dirhamnolipid ester – formation of reverse wormlike micelles in a binary (primerless) system

• David Liese,
• Hans Henning Wenk,
• Xin Lu,
• Jochen Kleinen and
• Gebhard Haberhauer

Beilstein J. Org. Chem. 2020, 16, 2820–2830, doi:10.3762/bjoc.16.232

• interaction of the alkyl chains. Keywords: dirhamnolipid ester; gemini surfactant; rheology; reverse wormlike micelle (RWLM); Introduction Surfactants have both hydrophilic and hydrophobic groups and are therefore amphiphilic molecules. Due to their unique molecular structure, surfactants are essential

Easy access to a carbohydrate-based template for stimuli-responsive surfactants

• Thomas Holmstrøm,
• Daniel Raydan and
• Christian Marcus Pedersen

Beilstein J. Org. Chem. 2020, 16, 2788–2794, doi:10.3762/bjoc.16.229

• surfactants: amphiphilic molecules that can alter their properties upon an external stimulus [6]. The intelligent surfactants are not passive but designed to undergo a molecular change when it is triggered with either a change in the pH value [7][8], upon light irradiation [9] or in the presence of metal ions

Morphology-tunable and pH-responsive supramolecular self-assemblies based on AB₂-type host–guest-conjugated amphiphilic molecules for controlled drug delivery

• Yang Bai,
• Cai-ping Liu,
• Di Chen,
• Long-hai Zhuo,
• Huai-tian Bu and
• Wei Tian

Beilstein J. Org. Chem. 2019, 15, 1925–1932, doi:10.3762/bjoc.15.188

Aqueous olefin metathesis: recent developments and applications

• Valerio Sabatino and
• Thomas R. Ward

Beilstein J. Org. Chem. 2019, 15, 445–468, doi:10.3762/bjoc.15.39

• on the catalytic activity of the reaction. In fact, catalyst and substrate are encapsulated into emulsion droplets formed in the reaction media above the aqueous layer, making the reaction proceed “on water” [21][22]. The introduction of amphiphilic molecules for aqueous micellar catalysis allows

Synthesis of new p-tert-butylcalix[4]arene-based polyammonium triazolyl amphiphiles and their binding with nucleoside phosphates

• Vladimir A. Burilov,
• Guzaliya A. Fatikhova,
• Mariya N. Dokuchaeva,
• Ramil I. Nugmanov,
• Diana A. Mironova,
• Pavel V. Dorovatovskii,
• Victor N. Khrustalev,
• Svetlana E. Solovieva and
• Igor S. Antipin

Beilstein J. Org. Chem. 2018, 14, 1980–1993, doi:10.3762/bjoc.14.173

• proposed structure of 10b. It should be noted that there are unexpected interactions of tert-butyl protons 2 with methylene protons 6 as well as between aromatic protons 1 with hydroxy protons 4 that can be attributed to a strong aggregation of the amphiphilic molecules in the solution. Aggregation

An amphiphilic pseudo[1]catenane: neutral guest-induced clouding point change

• Tomoki Ogoshi,
• Tomohiro Akutsu and
• Tada-aki Yamagishi

Beilstein J. Org. Chem. 2018, 14, 1937–1943, doi:10.3762/bjoc.14.167

• aggregation of the hydrophobic alkyl chain rings, which induced insolubilization of the bicyclic compound in aqueous media at 20 °C and a decrease in its clouding point. Keywords: amphiphilic molecules; host–guest complexes; lower critical solution temperature; pillar[n]arenes; pseudo[1]catenane

Nanoreactors for green catalysis

• M. Teresa De Martino,
• Loai K. E. A. Abdelmohsen,
• Floris P. J. T. Rutjes and
• Jan C. M. van Hest

Beilstein J. Org. Chem. 2018, 14, 716–733, doi:10.3762/bjoc.14.61

• section we will discuss the utility of some of the well-established catalytic nanoreactors towards green(er) chemistry [62]. 2.1. Micelles Micelles are supramolecular architectures that are assembled of amphiphilic molecules [41]. Above the critical micellar concentration (CMC), surfactants with the

• effect for hydrophobic substrates, which ensures higher reaction rates than those performed in bulk [63]. Besides, the structure of any micellar catalytic environment is governed by the arrangement of the amphiphilic molecules, creating, in many cases, a regioselective environment (Figure 1) that affects

Chemical systems, chemical contiguity and the emergence of life

• Terrence P. Kee and
• Pierre-Alain Monnard

Beilstein J. Org. Chem. 2017, 13, 1551–1563, doi:10.3762/bjoc.13.155

• -existing structures [94][95] has been experimentally exploited either by adding more amphiphiles at a pace that prevents the de novo formation of novel structures [17] or by adding amphiphile precursors that had to be converted within the structures into amphiphilic molecules themselves [83][96][97

Aggregation behaviour of a single-chain, phenylene-modified bolalipid and its miscibility with classical phospholipids

• Simon Drescher,
• Vasil M. Garamus,
• Christopher J. Garvey,
• Annette Meister and
• Alfred Blume

Beilstein J. Org. Chem. 2017, 13, 995–1007, doi:10.3762/bjoc.13.99

• behaviour; nanofibres; self-assembly; Introduction Bolalipids are amphiphilic molecules consisting of two hydrophilic headgroups attached to both ends of a long hydrocarbon spacer [1]. The hydrophobic spacer is composed of either a single alkyl chain or two chains connected via a glycerol moiety. These

Interactions between cyclodextrins and cellular components: Towards greener medical applications?

• Loïc Leclercq

Beilstein J. Org. Chem. 2016, 12, 2644–2662, doi:10.3762/bjoc.12.261

• complexes with various biomolecules including lipids, carbohydrates, proteins and nucleic acids. In this section, some biomolecule/CD inclusion complexes are presented. i) Complexation of lipids and consequences Lipids are hydrophobic or amphiphilic molecules very diverse, including, among other fats, waxes

• prenols, which are produced from condensation of isoprene units [54]. These compounds can be easily included inside the CDs because they are hydrophobic or amphiphilic molecules. As mentioned earlier, and as it will become exceeding clear throughout the following sections, the majority of research

Aggregation behaviour of amphiphilic cyclodextrins: the nucleation stage by atomistic molecular dynamics simulations

• Giuseppina Raffaini,
• Antonino Mazzaglia and
• Fabio Ganazzoli

Beilstein J. Org. Chem. 2015, 11, 2459–2473, doi:10.3762/bjoc.11.267

• distance from the aCD macrocycle c.o.m. calculated during the 500 ps MD run. The pairwise initial arrangements of two amphiphilic molecules that face the two hydrophobic H groups, the hydrophobic H and the polar P groups, and the two polar P groups, from left to right in the order. The colour codes are as

Synthesis of uniform cyclodextrin thioethers to transport hydrophobic drugs

• Lisa F. Becker,
• Dennis H. Schwarz and
• Gerhard Wenz

Beilstein J. Org. Chem. 2014, 10, 2920–2927, doi:10.3762/bjoc.10.310

• either nearly insoluble in water or the binding constants are rather low [32][33][34]. We focussed our effort on the design of hydrophilic and/or amphiphilic CD thioethers, because only amphiphilic molecules can form [35][36] or incorporate into bilayer membranes [37][38]. Amphiphilic CD carriers can

Supercritical carbon dioxide: a solvent like no other

• Jocelyn Peach and
• Julian Eastoe

Beilstein J. Org. Chem. 2014, 10, 1878–1895, doi:10.3762/bjoc.10.196

• through the addition of amphiphilic molecules, such as surfactants or polymers. The domains created are on the nanometer scale leading to the dispersions being transparent or translucent in appearance. The microemulsion appearance does not alter over time. Following this discovery, a vast array of

Thermotropic and lyotropic behaviour of new liquid-crystalline materials with different hydrophilic groups: synthesis and mesomorphic properties

• Alexej Bubnov,
• Miroslav Kašpar,
• Věra Hamplová,
• Ute Dawin and
• Frank Giesselmann

Beilstein J. Org. Chem. 2013, 9, 425–436, doi:10.3762/bjoc.9.45

• materials showing liquid-crystalline (LC) behaviour belong to two general classes: lyotropic materials, in which fluid anisotropy results from interactions between anisotropic aggregates of amphiphilic molecules; and thermotropic materials, in which the orientational order arises from interactions among

• systems composed of amphiphilic molecules can exhibit smectic phases with layered structure [2] or nematic (eventually cholesteric) phases. Lyotropic systems usually form a lamellar liquid-crystalline mesophase, i.e., a lyotropic analogue of the thermotropic orthogonal smectic A (SmA) phase [3], and more

Self-assembled organic–inorganic magnetic hybrid adsorbent ferrite based on cyclodextrin nanoparticles

• Ângelo M. L. Denadai,
• Frederico B. De Sousa,
• Joel J. Passos,
• Fernando C. Guatimosim,
• Kirla D. Barbosa,
• Ana E. Burgos,
• Fernando Castro de Oliveira,
• Jeann C. da Silva,
• Bernardo R. A. Neves,
• Nelcy D. S. Mohallem and
• Rubén D. Sinisterra

Beilstein J. Org. Chem. 2012, 8, 1867–1876, doi:10.3762/bjoc.8.215

• complexes [14][15][16][17]. Beyond these characteristics, it has been reported in the literature that CDs self-assemble into large aggregates [18][19][20], suggesting their uses as size-modulator molecules [21], similar to other amphiphilic molecules [22][23][24][25]. Based on these interesting properties

Differences between β-Ala and Gly-Gly in the design of amino acids-based hydrogels

• Andreea Pasc,
• Firmin Obounou Akong,
• Sedat Cosgun and
• Christine Gérardin

Beilstein J. Org. Chem. 2010, 6, 973–977, doi:10.3762/bjoc.6.109

• mechanism. On reducing the temperature to a certain value, amphiphilic molecules start to interact with each other by H-bonding to form micellar networks. The hydrophobicity of the 1D system is proportional to its length. Once the micellar fibre is too long, and thus too hydrophobic to be solubilised by

Pyridinium based amphiphilic hydrogelators as potential antibacterial agents

• Sayanti Brahmachari,
• Sisir Debnath,
• Sounak Dutta and
• Prasanta Kumar Das

Beilstein J. Org. Chem. 2010, 6, 859–868, doi:10.3762/bjoc.6.101

• properties to amphiphilic molecules [28][29][30][31]. The cationic charge of the amphiphile plays an instrumental role in disrupting the innate defense mechanism of microorganisms by disrupting the microbial cell membrane [32][33]. Hence, it would be interesting to develop amphiphilic hydrogelators that have

• factors for the gelation process were found to be non-covalent interactions such as π–π stacking and intermolecular hydrogen bonding. These cationic amphiphilic molecules exhibited antibacterial activity against both Gram-positive and Gram-negative bacteria and were found to be viable towards mammalian