16669-54-8Relevant academic research and scientific papers
Synthesis of new macrobicyclic hexaamide ligands
Mo, Zunli,Yang, Wu,Gao, Jinzhang,Chen, Hong,Gong, Qiaojuan,Hou, Jingguo,Kang, Jingwan
, p. 3503 - 3508 (1998)
A new two-step synthesis method of macrobicyclic hexaamide ligands LH6 (I and II) with double condensation of triethyl nitrilotriacetate and 1,4(1,2)-diaminobenzene was developed. The cyclization does not require high dilution and template techniques. Two new hexaamide ligands were prepared in good yields according to the proposed method.
Synthesis of a new macrocyclic ligand with six amide receptor sites
Bhattacharjee, Manish,Datta, Riya
, p. 3579 - 3580 (1996)
The macrobicyclic hexaamide ligand LH6 has been synthesized from double condensation of triethyl ester of nitrilotriacetic acid and 1,2-diaminobenzene in 60% yield.
Connector ability to design superhydrophobic and oleophobic surfaces from conducting polymers
Zenerino, Arnaud,Darmanin, Thierry,Taffin De Givenchy, Elisabeth,Amigoni, Sonia,Guittard, Frederic
, p. 13545 - 13549 (2010)
In the aim of creating superoleophobic surfaces using monomers with short perfluorinated chains, to avoid drawbacks associated with PFOA, original semifluorinated (C4F9, C6F13) 3,4-ethylenedioxypyrrole derivatives were synthesized. These monomers were obtained using the faster synthetic method than previously described with some analogues, characterized and electrochemically polymerized on gold plates. The obtained surfaces exhibited superhydrophobic (contact angle with water of 157° and 158°, respectively) and oleophobic properties (contact angle with hexadecane: 88° and 108°, respectively). The comparison between these new monomers and already published analogue EDOP6 confirms the importance of the bipolaronic form of conductive polymer for obtaining surface nanoporosity and as a consequence improving surface oleophobicity. Thus, little change in the molecule design of the connector and the spacer of the monomer can have a significant influence on the surface oleophobicity.
Friction modifier and their use in lubricants and fuels
-
Page/Page column 29, (2016/01/09)
A non-aqueous lubricating composition containing a major amount of an oil of lubricating viscosity and a minor amount, in the range of 0.02% to 5% by weight, of at least one compound represented by the structural formula (I): wherein R4 represents H or a C1 to C9 hydrocarbyl group or x, y and z are independently integers in the range 1 to 6; and R1, R2 and R3 each independently represent a C1 to C10 hydrocarbyl or substituted hydrocarbyl group.
Photocurable resin composition, dry film thereof, pattern forming method, and electrical/electronic part protective film
-
, (2012/05/04)
A photocurable composition includes: (A) an epoxy group-containing polymer compound having repeating units represented by the following formula (1), where R1 to R4 are each a hydrocarbon group, m is an integer of 1 to 100, a, b, c and d are each 0 or a positive number, such that 0 (c+d)/(a+b+c+d) ≤ 1.0, and X and Y are each the formula (2) or (3), provided that at least one group of the formula (3) is present, (B) a photoacid generator represented by the formula (8) and (C) a solvent.
Resist composition and patterning process
-
, (2010/02/17)
The present invention relates to: a resist composition such as a chemically amplified resist composition for providing an excellent pattern profile even at a substrate-side boundary face of resist, in addition to a higher resolution in photolithography for micro-fabrication, and particularly in photolithography adopting, as an exposure source, KrF laser, ArF laser, F2 laser, ultra-short ultraviolet light, electron beam, X-rays, or the like; and a patterning process utilizing the resist composition. The present invention provides a chemically amplified resist composition comprising one or more kinds of amine compounds or amine oxide compounds (except for those having a nitrogen atom of amine or amine oxide included in a ring structure of an aromatic ring) at least having a carboxyl group and having no hydrogen atoms covalently bonded to a nitrogen atom as a basic center.
POSITIVE RESIST COMPOSITION AND PATTERNING PROCESS
-
, (2010/04/23)
A positive resist composition comprises (A) a resin component which becomes soluble in an alkaline developer under the action of an acid and (B) an acid generator. The resin (A) is a polymer comprising recurring units containing a non-leaving hydroxyl group represented by formula (1) wherein R1 is H, methyl or trifluoromethyl, X is a single bond or methylene, m is 1 or 2, and the hydroxyl group attaches to a secondary carbon atom. The composition is improved in resolution when processed by lithography.
Photoacid generators, chemically amplified resist compositions, and patterning process
-
, (2008/06/13)
A photoacid generator has formula (1). A chemically amplified resist composition comprising the photoacid generator has advantages including a high resolution, focus latitude, long-term PED dimensional stability, and a satisfactory pattern profile shape.
N-SUBSTITUTED 3,4-ALKYLENEDIOXYPYRROLES, ESTER SUBSTITUTED DIHYDROXYPYRROLES AND METHODS FOR SYNTHESIS OF THESE PYRROLES
-
Page/Page column 13, (2008/06/13)
A family of N-substituted 3,4-allcylenedioxypyrrole includes monomers for of formula (I) electropolymerization to conjugated polymers and key intermediates for the preparation of the monomers. The preparation of the //-substituted 3,4-aJkylenedioxypyrτole
Iron porphyrins catalyze the synthesis of non-protected amino acid esters from ammonia and diazoacetates
Aviv, Iris,Gross, Zeev
, p. 4477 - 4479 (2008/09/19)
Iron complexes of porphyrins (and corroles to a lesser extent) are the first catalysts to utilize ammonia for the synthesis of N-free amino acid esters. The Royal Society of Chemistry 2006.
