1974
DOI: 10.1007/bf00617293
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Infrared and ultraviolet spectra of polyphenyl ether and intermediate compounds of the process of synthesis

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“…FT-IR analysis shows the successful halogen-metal-exchange of 4,4’-dibromobiphenyl in all three cases, according to the absence of ν s (C-Br) at 671 cm -1­ and ν as (C-Br) at 760 cm -1 in the EOF-spectra ( Figure 2 ) [ 17 , 18 ]. The signals at 2950 cm -1 indicate an aliphatic substitution of tin, antimony or bismuth as a result of the lithiation with n -butyllithium and therefore residual reactive molecules at the moment of the framework formation.…”
Section: Resultsmentioning
confidence: 99%
“…FT-IR analysis shows the successful halogen-metal-exchange of 4,4’-dibromobiphenyl in all three cases, according to the absence of ν s (C-Br) at 671 cm -1­ and ν as (C-Br) at 760 cm -1 in the EOF-spectra ( Figure 2 ) [ 17 , 18 ]. The signals at 2950 cm -1 indicate an aliphatic substitution of tin, antimony or bismuth as a result of the lithiation with n -butyllithium and therefore residual reactive molecules at the moment of the framework formation.…”
Section: Resultsmentioning
confidence: 99%