22657-66-5

Upstream product

• 108-94-1 cyclohexanone 
• 87-62-7 2,6-dimethylaniline 

Downstream Products

• 169179-52-6 N,N'-bis<4-<1-(4-amino-3,5-dimethylphenyl)cyclohexyl>-2,6-dimethylphenyl>-5-tert-butylisophthalamide 
• 172788-71-5 N-<4-<1-(4-Amino-3,5-dimethylphenyl)cyclohexylidene>-2,6-dimethylphenyl>-3-<<4-<1-(4-amino-3,5-dimethylphenyl)cyclohexylidene>-2,6-dimethylphenyl>sulfonyl>benzamide 
• 231613-64-2 N,N'-bis{4-[-(4-amino-3,5-dimethylphenyl)cyclohexyl]-2,6-dimethylphenyl}benzene-1,3-diacetamide 
• 231613-63-1 N,N'-bis[4-[-(4-amino-3,5-dimethylphenyl)cyclohexyl]-2,6-dimethylphenyl]homoisophthalamide 
• 252641-90-0 C₆H₁₀(C₆H₂(CH₃)2NHC(O)C₅H₃NC(O)NHC₅H₂(CH₃)2N)2 
• 299173-87-8 N-{4-[1-(4-amino-3,5-dimethyl-phenyl)-cyclohexyl]-2,6-dimethyl-phenyl}-N'-(2,6-diisopropyl-phenyl)-isophthalamide 
• 141062-51-3 N,N'-bis{4-[1-(4-amino-3,5-dimethylphenyl)cyclohexylidene]-2,6-dimethylphenyl}isophthalic acid diamide 
• 299173-86-7 N-{4-[1-(4-amino-3,5-dimethyl-phenyl)-cyclohexyl]-2,6-dimethyl-phenyl}-4-tert-butyl-benzamide 
• 402912-73-6 N-(9-anthranoylcarboxy)-{1,1-bis[(4-amino-3,5-dimethyl)phenyl]cyclohyxane} 
• 643013-63-2 C₂₂H₂₆I₂ 

Relevant academic research and scientific papers

The effect of the linker size in C2-symmetrical chiral ligands on the self-assembly formation of luminescent triple-stranded di-metallic Eu(iii) helicates in solution

Chiral lanthanide-based supramolecular structures have gained significant importance in view of their application in imaging, sensing and other functional purposes. We have designed chiral C2-symmetrical ligands (L) based on the use of two 2,6-

COLORED COMPOSITION, INKJET RECORDING INK, AND INKJET RECORDING METHOD

It is an object to provide a coloring composition which is excellent in moisture resistance, and is also excellent in hue, saturation and ozone resistance. Further, it is an object to provide an ink for inkjet recording, which includes the coloring composition, and an inkjet recording method using the ink for inkjet recording. A coloring composition including the compound represented by Formula (1) described in the specification and the compound selected from (A) to (C) described in the specification.

NOVEL COMPOUND HAVING MULTIMER STRUCTURE OF XANTHENE DERIVATIVE, COLORING COMPOSITION, INK FOR INKJET RECORDING, METHOD OF INKJET RECORDING, COLOR FILTER, AND COLOR TONER

There is provided a compound represented by formula (1): in formula (1), L represents a divalent to tetravalent linking group; D represents a residue obtained by removing 1 to 5 hydrogen atoms from a compound represented by formula (2); m represents an integer of 1 to 10, however, each L may be the same with or different from every other L; n represents an integer of 2 to 10, however, each D may be the same with or different from every other D; and in formula (2), each of R4 to R24 independently represents a hydrogen atom or a substituent, provided that formula (2) has at least one or more ionic hydrophilic groups.

Fluorescent perylene diimide rotaxanes: Spectroscopic signatures of wheel-chromophore interactions

[2]- and [3]-rotaxanes with a tetraphenoxy perylene diimide core were synthesized. Hydrogen bonding between the wheel and the imide changes the optical properties of the perylene chromophore: the absorption and fluorescence spectra are red-shifted. The decay times of the rotaxanes are shorter in comparison with that of the axle. Single molecule fluorescence measurements reveal relatively narrow distributions of emission maxima and decay times. The averages are in agreement with ensemble measurements. The observed red shifts make the perylene diimide a suitable chromophore for sensing the position of the wheel on the axle.

Energy transfer labels with mechanically linked fluorophores

Mechanically linked energy transfer labels comprising at least one donor fluorophore, at least one acceptor fluorophore, and at least one support member, wherein steric interactions between the donor fluorophore(s), the acceptor fluorophore(s), and/or the support member(s) induce non-covalent association between the fluorophores and the support member(s), thereby forming a three-dimensional macromolecular structure which mechanically links the donor fluorophore(s) and the acceptor fluorophore(s). Fluorescence resonance energy transfer (FRET) occurs from donor fluorophore to acceptor fluorophore through space. No direct connectivity with covalent bonds exists between the fluorophores. Instead, mechanical barriers hold the donor/acceptor fluorophores in place during the FRET process.

Synthesis and structure elucidation of a new [2]-catenane

A supramolecular self-assembly process has lead to the synthesis of new type of [2]-catenane. A 34% yield of catenane was obtained from a one-pot macrocyclization reaction. Its three-dimensional structure was by using two-dimensional 1H NMR spe

Molecular Recognition of p-Benzoquinone by a Macrocyclic Host

The design, synthesis and molecular recognition properties of a new macrocyclic host which specifically complexes p-benzoquinone using four H-bonds and four edge-to-face ?-? interactions are reported.