1985
DOI: 10.1007/978-3-662-02429-4
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Phenolic Resins

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Cited by 377 publications
(164 citation statements)
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“…The 13 (Figure 3). 1,33,35,36 These results confirmed that 2 contains arylene-methylene units, as shown in Scheme 1; moreover, some repeating units possessed acetoxymethyl moieties, which were formed by the condensation of acetic acid and methylol moieties, as described in our previous report. 33 Reactive novolac with a methylol group (3)…”
Section: Addition-condensation Of 22-bis(4-methoxyphenyl)propane (1)supporting
confidence: 87%
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“…The 13 (Figure 3). 1,33,35,36 These results confirmed that 2 contains arylene-methylene units, as shown in Scheme 1; moreover, some repeating units possessed acetoxymethyl moieties, which were formed by the condensation of acetic acid and methylol moieties, as described in our previous report. 33 Reactive novolac with a methylol group (3)…”
Section: Addition-condensation Of 22-bis(4-methoxyphenyl)propane (1)supporting
confidence: 87%
“…A volume of 1 mol l À1 KOH aqueous (2.0 ml) was added to a solution of 2 (0.28 g) in THF (3 ml), and the mixture was stirred at ambient temperature for 72 h. The mixture was poured into methanol (100 ml) to obtain the desired polymer (3). 1 Cure reaction between 3 and 4. The typical procedure for the cure reaction of 3 and 4 is as follows: 3 and 4 were dissolved in THF, and the solution was stirred for 1 h. The mixture was heated at 130 1C for several hours to vaporize solvent and water, and to carry out the cure reaction.…”
Section: Methodsmentioning
confidence: 99%
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