Freestanding organogels by molecular velcro of unsaturated amphiphiles.

A simple amphiphile, N-cardanyltaurine amide (NCT) with different degrees of cis-unsaturation in its tail resulted in the formation of strong organogels. Interestingly, this is in contrast to the commonly accepted notion that introducing unsaturation in alkyl chains enhances fluidity in lipid assemblies. The physico-chemical and first-principles DFT calculations confirmed the pegging of 'kinked' unsaturated side chains, where the hydrophobic interlocking as in Velcro fasteners leads to a network of cylindrical micelles, resulting in self-standing organogels. Textural profile analysis and spectroscopic details substantiated the dynamic assembly to resemble a 3D network of gelators rather than being a cross-linked or polymerized matrix of monomers.

In Situ Synthesis of Metal Nanoparticle Embedded Hybrid Soft Nanomaterials.

The allure of integrating the tunable properties of soft nanomaterials with the unique optical and electronic properties of metal nanoparticles has led to the development of organic-inorganic hybrid nanomaterials. A promising method for the synthesis of such organic-inorganic hybrid nanomaterials is afforded by the in situ generation of metal nanoparticles within a host organic template. Due to their tunable surface morphology and porosity, soft organic materials such as gels, liquid crystals, and polymers that are derived from various synthetic or natural compounds can act as templates for the synthesis of metal nanoparticles of different shapes and sizes. This method provides stabilization to the metal nanoparticles by the organic soft material and advantageously precludes the use of external reducing or capping agents in many instances. In this Account, we exemplify the green chemistry approach for synthesizing these materials, both in the choice of gelators as soft material frameworks and in the reduction mechanisms that generate the metal nanoparticles. Established herein is the core design principle centered on conceiving multifaceted amphiphilic soft materials that possess the ability to self-assemble and reduce metal ions into nanoparticles. Furthermore, these soft materials stabilize the in situ generated metal nanoparticles and retain their self-assembly ability to generate metal nanoparticle embedded homogeneous organic-inorganic hybrid materials. We discuss a remarkable example of vegetable-based drying oils as host templates for metal ions, resulting in the synthesis of novel hybrid nanomaterials. The synthesis of metal nanoparticles via polymers and self-assembled materials fabricated via cardanol (a bioorganic monomer derived from cashew nut shell liquid) are also explored in this Account. The organic-inorganic hybrid structures were characterized by several techniques such as UV-visible spectroscopy, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Utilization of silver nanoparticle-based hybrid nanomaterials as an antimicrobial material is another illustration of the advantage of hybrid nanomaterials. We envision that the results summarized in this Account will help the scientific community to design and develop diverse organic-inorganic hybrid materials using environmentally benign methods and that these materials will yield advanced properties that have multifaceted applications in various research fields.

A common tattoo chemical for energy storage: henna plant-derived naphthoquinone dimer as a green and sustainable cathode material for Li-ion batteries.

The burgeoning energy demands of an increasingly eco-conscious population have spurred the need for sustainable energy storage devices, and have called into question the viability of the popular lithium ion battery. A series of natural polyaromatic compounds have previously displayed the capability to bind lithium via polar oxygen-containing functional groups that act as redox centers in potential electrodes. Lawsone, a widely renowned dye molecule extracted from the henna leaf, can be dimerized to bislawsone to yield up to six carbonyl/hydroxyl groups for potential lithium coordination. The facile one-step dimerization and subsequent chemical lithiation of bislawsone minimizes synthetic steps and toxic reagents compared to existing systems. We therefore report lithiated bislawsone as a candidate to advance non-toxic and recyclable green battery materials. Bislawsone based electrodes displayed a specific capacity of up to 130 mA h g-1 at 20 mA g-1 currents, and voltage plateaus at 2.1-2.5 V, which are comparable to modern Li-ion battery cathodes.

Reversible Switching of Tb(III) Emission by Sensitization from 2,3-Dihydroxynaphthalene in an Isothermally Reversible Ionic Liquid.

A reversible room-temperature ionic liquid (ILO) was prepared by the addition of CO2 to an equimolar mixture of hexylamidine (AD) and butylamine (AN). The ILO and AD/AN mixture were cycled repeatedly by alternating the passage of CO2 and N2 gases through the liquid. The ILO was utilized to sensitize very efficiently energy transfer to and emission by Tb(III) ions when 2,3-dihydroxynaphthalene (DHN) was irradiated. The emission was nearly completely quenched in the AD/AN mixture. The process described here is unique in its use of CO2 and N2 to "switch on and off" the emission by a lanthanide ion, Tb(III) in this case. In the corresponding amidinium dithiocarbamate ionic liquid (ILS), no appreciable Tb(III) emission was found due to quenching of the excited singlet state of DHN by thio groups. The ILS was not reconverted to the AD/AN mixture upon adding N2; N2 bubbling did not result in the displacement of CS2.

A fluorescent molecular probe for the identification of zinc and cadmium salts by excited state charge transfer modulation.

A fluorescent probe for the identification of a given metal salt is not known. Herein we present a new fluorescent probe 1 for the identification of different zinc and cadmium salts by exploiting the effect of the charge density of counteranions to perturb the excited state solvatochromic behavior of the probe.

Chain folding controlled by an isomeric repeat unit: helix formation versus random aggregation in acetylene-bridged carbazole-bipyridine co-oligomers.

An unprecedented, positional effect of the isomeric repeat unit on chain folding in donor­acceptor-linked oligomers, which contain alternating bipyridine and carbazole moieties that are connected through an acetylinic linkage, is reported. 4,4'-Linked oligomer 1 adopts an intrachain helical conformation (CD-active) in CHCl3/MeCN (20:80 v/v), whereas oligomer 2, which contains an isomeric 6,6'-linkage, forms interchain randomly coiled aggregates (CD-inactive). The substitution position plays a significant role in controlling the variations in electronic effects and dipole moments around the bipyridyl moiety, which are responsible for this observed phenomenon. Two model compounds of oligomers 1 and 2 (3 and 4, respectively) were prepared and their properties were compared. A systematic investigation of the photophysical and CD properties of these structures, as well as theoretical studies, support our conclusions.

Solvent-induced aggregation and cation-controlled self-assembly of tripodal squaraine dyes: optical, chiroptical and morphological properties.

The synthesis, characterisation, optical, chiroptical, aggregation, and alkaline earth metal cation assisted self-assembly properties of tripodal squaraine dyes have been described. In the tripodal geometry, these dyes exhibit three absorption bands around 650, 620 and 580 nm in contrast to the single, sharp absorption of a simple dye (SQ) at 640 nm. The fluorescence quantum yield of the squaraine dyes are 25-30 times lower when compared to that of SQ, which indicates intramolecular exciton interaction as a result of the confinement of the dyes. The evaporation of an acetonitrile solution of the dye resulted in the formation of vesicular objects as confirmed by AFM and TEM analyses. However, evaporation of an acetonitrile solution containing 10-12 % water gave short fibrous aggregates. In the presence of Ca(2+) or Mg(2+) ions, the dyes exhibit an intense and sharp absorption band at 547 nm with a concomitant decrease of the native absorption. Interestingly, the dye with chiral groups failed to give a circular dichroic signal during aggregation in solvent mixtures, whereas strong signals were observed in the presence of Ca(2+) and Mg(2+) ions. AFM and TEM analyses of the corresponding cation complexes revealed the formation of worm like nanohelices. However, addition of EDTA to the Ca(2+) or Mg(2+) complex exhibited a reversal of the absorption, emission, and circular dichroic spectra to that of the native dye, indicating decomplexation. AFM analyses revealed the transformation of the helices to particles. These observations reveal the difference in the nature and properties of the simple aggregates formed in solvent mixtures and those formed in the presence of cations. In the present study, we were able to establish the importance of specific cation binding in controlling the size, shape, and properties of the hierarchical assemblies of tripodal squaraines.