102310-68-9

Upstream product

• 109-65-9 1-bromo-butane 
• 99-24-1 methyl galloate 
• 149-91-7 3,4,5-trihydroxybenzoic acid 

Downstream Products

• 232269-63-5 C₁₉H₃₂O₄ 
• 1269010-36-7 3-(3,4,5-tributoxyphenyl)-5-(2-pyridyl) pyrazole 
• 1269010-30-1 1-(3,4,5-tributoxyphenyl)ethanone 
• 1350321-19-5 C₆H₃(OH)2CHNNHCOC₆H₂(OCH₂CH₂CH₂CH₃)3 
• 1245932-82-4 C₄₈H₆₈O₁₀ 
• 102657-75-0 3,4,5-tris(n-butan-1-yloxy)benzoyl chloride 
• 102020-55-3 3,4,5-tris(n-butan-1-yloxy)benzoic acid 

Relevant academic research and scientific papers

Tweaking a BODIPY Spherical Self-Assembly to 2D Supramolecular Polymers Facilitates Excited-State Cascade Energy Transfer

Excited state properties such as emission, exciton transport, electron transfer, etc., are strongly dependent on the shape, size and molecular arrangement of chromophore based supramolecular architectures. Herein, we demonstrate creation and control of distinct supramolecular energy landscapes for the reversible control of the excited-state emission processes through cascade energy transfer in chromophore assemblies, facilitated by an unprecedented solvent effect. In methylcyclohexane, a tailor-made Y-shaped BODIPY derivative self-assembles to form an unusual spherical architecture of 400–1200 nm size, which exhibits a single emission at 540 nm upon 475 nm excitation through a normal excitation deactivation process. However, in n-decane, the same BODIPY derivative forms two-dimensional supramolecular sheets, exhibiting multiple emission peaks at 540, 610, 650, 725 and 790 nm with 475 nm excitation due to cascade energy transfer. Further control on the morphology and excitation energy transfer is possible with variable solvent composition and ultrasound stimulation, resulting in enhanced near-infrared emission with an overall pseudo Stokes shift of 7105 cm?1.

Fluorescent columnar bis(boron difluoride) complexes derived from tetraketonates

Three new series of bis-(boron difluoride) complexes 1a-c derived from substituted tetraketonates 2a-c are reported, and their mesomorphic and optical properties have been investigated. Two single crystals of mesogenic ligand 2a (n = 6) and nonmesogenic d

Mesomorphism and luminescence properties of platinum(II) complexes with tris(alkoxy)phenyl-functionalized pyridyl pyrazolate chelates

A series of new mesomorphic platinum(II) complexes 1-4 bearing pyridyl pyrazolate chelates are reported herein. In this approach, pyridyl azolate ligands have been strategically functionalized with tris(alkoxy)phenyl groups with various alkyl chain length

Decorating the lanthanide terminus of self-assembled heterodinuclear lanthanum(iii)/gallium(iii) helicates

Arylacylhydrazones of 2,3-dihydroxybenzaldehyde are appropriate ligands for the preparation of heterodinuclear triple-stranded helicates involving high coordinated lanthanide(iii) ions. In the present study, three different kinds of substituents are intro

Influence of alkoxy tail length on the phase behaviour of mesogen-jacketed liquid crystalline polymers with fan-shaped pendants

A series of new monomers of 2, 5-bis [(3, 4, 5-trialkoxy benzyl) oxycarbonyl] styrene (denoted as M-tri-OCmH2m + 1, m = 1, 2, 4, 6, 8, 10, 12, where m indicated the number of carbon atoms in the alkoxy group) were designed and synthesized. Then, their corresponding polymers P-tri-OCmH2m + 1 (m = 1, 2, 4, 6, 8, 10, 12) were synthesized by free radical polymerization. The chemical structure of the monomers was confirmed by elemental analysis, 1H NMR and 13C NMR. The molecular characterization of polymers was performed with 1H NMR, gel permeation chromatography (GPC). The thermal stability of polymers was investigated by thermogravimetric analysis (TGA). The phase structure and transition behaviours were studied using differential scanning calorimetry (DSC), polarized light microscopy (PLM), one- and two-dimensional (1D and 2D) wide-angle X-ray diffraction (WAXD). We found that P-tri-OCmH2m + 1 (m = 1, 2) with short n-alkoxy substituents as the tail form columnar nematic (ΦN) phase; that with the increasing length of alkoxy tails, P-tri-OCmH2m + 1 (m = 4, 6, 8) can demonstrate the hexagonal columnar (ΦH) phase; however, when the length of alkoxy tails exceeded a threshold, P-tri-OCmH2m + 1 (m = 10, 12) only develop into columnar nematic (ΦN) phase instead of ΦH phase.

Elucidating the structure of the pm3n cubic phase of supramolecular dendrimers through the modification of their aliphatic to aromatic volume ratio

The synthesis, and structural and retrostructural analysis of a library of second-generation conical dendrons that self-assemble into spherical supramolecular dendrimers is reported. This library consists of amphiphilic dendrons with n-alkyl groups contai

Molecular control of macroscopic cubic, columnar, and lamellar organizations in luminescent lanthanide-containing thermotropic liquid crystals

The connection of lipophilic gallic acid derivatives at the 5,5′- or 6,6′-positions of the rigid 2,6-bis(1-ethyl-benzimidazol-2-yl)pyridine core provides two pro-mesogenic tridentate ligands L10 and L12, whose molecular shapes, anisometries, and directional intermolecular π-stacking can be tuned. X-ray diffraction data in the crystalline state, combined with solution 1H NMR measurements, show that complexation with trivalent lanthanides, Ln(III), produces the neutral hemi-disklike complexes [Ln(Li)(NO3)3] (i = 10, 12), which dimerize to give the rodlike bimetallic complexes [Ln2(Li)2(NO 3)6] at lower temperature. The relevant thermodynamic parameters for the latter process depend on the nature of the ligand, the size of the metal ion, and the strength of the intermolecular interactions involved in the condensed phase. These three-dimensional models obtained for the complexes in the crystals and in solution are eventually confronted with small-angle XRD profiles recorded in the intermediate thermotropic liquid crystalline phase, in which the rigidity of the packed polyaromatic cores is maintained, while the alkyl chains are molten. According to the specific geometries and nuclearities of the molecular complexes, three types of mesophases (lamellar, columnar, and cubic) can be induced, which provides a direct correlation between the microscopic arrangements and the macroscopic ordering in lanthanide-containing metallomesogens.

Depigmenting activity and low cytotoxicity of alkoxy benzoates or alkoxy cinnamte in cultured melanocytes

To obtain effective and safe topical depigmenting agents, we synthesized hydroxybenzoates, alkoxybenzoates, and 3,4,5-trimethoxycinnamate containing a thymol moiety and screened then for high-level inhibitory activity against melanin synthesis in cultured melanocytes. Eight compounds were tested for their depigmenting effect and cytotoxicity using a murine melanocyte cell line. We found that 3,4,5-trialkoxybenzoates and 3,4,5-trimethoxycinnamate, synthesized by conjugating 3,4,5-trialkoxybenzoic acids and 3,4,5-trimethoxycinnmic acid with thymol, showed a potent depigmenting effect and low cytotoxicity. Compound 4h, 5-methyl-2-(methylethyl)phenyl (2E)-3-(3,4,5-trimethoxyphenyl)prop-2-enoate, showed the most potent depigmenting effect (IC50=10 μM) with low cytotoxicity (IC50=200 μM).

Metallomesogens by ligand design

In this Perspective, some of the basic principles of ligand design will be described as they apply to the synthesis of metal complexes with liquid crystal properties. Liquid crystal properties of metal complexes are a delicate function of both ligand and metal and examples will be chosen to illustrate this statement. In particular, the effect of the metal complex moiety on the mesomorphism of a series of imine and diimine liquid crystals is described. The Royal Society of Chemistry 2003.

Coassembly of a hexagonal columnar liquid crystalline superlattice from polymer(s) coated with a three-cylindrical bundle supramolecular dendrimer

The synthesis and structural analysis of a polymer containing twin- dendritic benzamide side-groups (i.e. poly{N-[3,4-bis(n-dodecan-1-yloxy)- 5(1-methacryloyl-η-undecan-1-yloxy)phenyl]-3,4,5-tris(n-dodecan-1- yloxy)benzamide}) (19) are described. The disc