82194-56-7Relevant academic research and scientific papers
DEVELOPER FOR THERMAL RECORDING MATERIAL AND THERMAL RECORDING MATERIALS
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, (2008/06/13)
The developer for a thermal recording material of the present invention comprises a condensed composition consisting of, of condensates represented by the formula (1): wherein R is a hydrogen atom, a hydroxyl group, a lower alkyl group having 1 to 5 carbon atoms, an alkoxyl group having 1 to 5 carbon atoms, an aryl group or an aralkyl group, R in the number of m may be the same or different and m is an integer of 0-3, X and Y are each a hydrogen atom, an alkyl group or an aryl group, provided that at least one of X an dY is an alkyl group or an aryl group, and n is an integer of 0-3, a condensate having two cores wherein n="0 or a condensed composition comprising a condensate having two cores wherein" n=0 as a main component, and at least one kind of condensate of the formula wherein n=1-3 (3-5 core condensate). The developer for thermal recording materials of the present invention is applied to a heat-coloring layer of thermal recording materials, along with a basic dye (preferably further with a sensitizer). According to the present invention, a developer for thermal recording materials, which is capable of realizing a thermal recording material capable of affording high colored image density and superior in preservation stability (particularly heat resistance and moisture resistance) of recorded images and non-image areas, while satisfying recent requirements for high sensitivity, can be obtained.
Regiospecificity in Reactions of Metal Phenoxides. Synthesis of 2,2'-alkylidenebisphenols
Casiraghi, Giovanni,Casnati, Giuseppe,Pochini, Andrea,Ungaro, Rocco
, p. 805 - 808 (2007/10/02)
The reactions between aryloxymagnesium bromides (1) with linear aliphatic aldehydes (2) and their acetals (10) in aprotic solvents of variable donicity have been investigated.In benzene high ortho-regiospecificity is observed in all cases, although with the aldehyde (2) the yield of 2,2'-alkylidenebisphenols (5) is usually low because of the competing aldehyde self-condensation.This process is avoided using diethyl acetals as electrophilic reagents which give the products (5) in good yields.
