An in-depth mechanistic investigation of the radical initiation behavior of monoacylgermanes
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DOI: 10.1021/acs.macromol.7b01721
Abstract: Five para-substituted monoacyltrimethylgermane derivatives, i.e., p-fluorobenzoyltrimethylgermane (pFBG, λmax = 405 nm), p-methoxybenzoyltrimethylgermane (pMBG, λmax = 397 nm), benzoyltrimethylgermane (pHBG, λmax = 409 nm), p-cyanobenzoyltrimethylgermane (pCBG, λmax = 425 nm), and p-nitrobenzoyltrimethylgermane (pNBG, λmax = 429… read more here.
Keywords: investigation radical; initiation; initiation behavior; depth mechanistic ... See more keywords