1971
DOI: 10.1016/0022-2364(71)90073-4
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The indirect measurement of 11BH coupling constants in some organoboron compounds

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Cited by 3 publications
(1 citation statement)
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“…In the 1 H NMR spectra of K [3] and K [4] the signals of methoxy groups are shifted to high field in comparison with 1 and 2 up to 3.22 and 3.17 ppm, respectively, and appear as 1:1:1:1 quartets due to long-range B-H coupling ( 3 J B,H = 3.7-3.8 Hz). Such coupling has also been previously observed for some organoboron compounds [29][30][31][32], methylsulfanyl derivatives of the closo-dodecaborate anion [33,34] and B-methysulfanyl derivatives of cobalt bis(dicarbollide) anion [35].…”
Section: Resultssupporting
confidence: 74%
“…In the 1 H NMR spectra of K [3] and K [4] the signals of methoxy groups are shifted to high field in comparison with 1 and 2 up to 3.22 and 3.17 ppm, respectively, and appear as 1:1:1:1 quartets due to long-range B-H coupling ( 3 J B,H = 3.7-3.8 Hz). Such coupling has also been previously observed for some organoboron compounds [29][30][31][32], methylsulfanyl derivatives of the closo-dodecaborate anion [33,34] and B-methysulfanyl derivatives of cobalt bis(dicarbollide) anion [35].…”
Section: Resultssupporting
confidence: 74%