1968
DOI: 10.1007/bf00907801
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IR and PMR spectra of some arene ?-complexes of chromium

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Cited by 3 publications
(2 citation statements)
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“…This is illustrated in the case of 2; the aromatic protons are at δ 4.19 (in contrast to 7.23 for ethylbenzene) ; the C H 2 protons give a quadruplet (J = 7.5 Hz) centered at δ 2.30 (2.68 for ethylbenzene); the C H 3 protons give a triplet (J = 7.5 Hz) centered at δ 1.10 (1.25 for ethyl benzene) [26]. This is illustrated in the case of 2; the aromatic protons are at δ 4.19 (in contrast to 7.23 for ethylbenzene) ; the C H 2 protons give a quadruplet (J = 7.5 Hz) centered at δ 2.30 (2.68 for ethylbenzene); the C H 3 protons give a triplet (J = 7.5 Hz) centered at δ 1.10 (1.25 for ethyl benzene) [26].…”
Section: -2)mentioning
confidence: 98%
“…This is illustrated in the case of 2; the aromatic protons are at δ 4.19 (in contrast to 7.23 for ethylbenzene) ; the C H 2 protons give a quadruplet (J = 7.5 Hz) centered at δ 2.30 (2.68 for ethylbenzene); the C H 3 protons give a triplet (J = 7.5 Hz) centered at δ 1.10 (1.25 for ethyl benzene) [26]. This is illustrated in the case of 2; the aromatic protons are at δ 4.19 (in contrast to 7.23 for ethylbenzene) ; the C H 2 protons give a quadruplet (J = 7.5 Hz) centered at δ 2.30 (2.68 for ethylbenzene); the C H 3 protons give a triplet (J = 7.5 Hz) centered at δ 1.10 (1.25 for ethyl benzene) [26].…”
Section: -2)mentioning
confidence: 98%
“…It is also present in many pharmaceutical products due to its ability to stabilize blood sugar level 20. For these reasons many scientists keep trying to prepare novel compounds that containing chromium, especially coordination compounds 21–26…”
Section: Introductionmentioning
confidence: 99%