1974
DOI: 10.1039/c39740000518
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Absence of the expected field effect in the hydrogen-isotope exchange reactions of a bridged anthracene derivative carrying a nitrogen pole

Abstract: In hydrogen-isotope exchange, the overall reactivities of the two aromatic rings of the conjugate acid of 9,10-dihydro-9,10-(trans-1 1-amino-12-methylethano)anthracene (111) are the same, in spite of the fact that the nitrogen pole is much nearer one ring than the other.

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“…Similarly, the FAB spectrum taken on the products of the reaction of NRe(OEP) with ClCr(TTP) and ClCr(OEP) gave clusters centered at 1453.4 and 1317.6, the value expected for {(OEP)ReNCr(TTP)} + and {(OEP)-ReNCr(OEP)} + , respectively. Although other heterobimetallic µ-nitrido complexes have been reported, 16,17,[21][22][23] this is the first account of porphyrin containing complexes.…”
mentioning
confidence: 99%
“…Similarly, the FAB spectrum taken on the products of the reaction of NRe(OEP) with ClCr(TTP) and ClCr(OEP) gave clusters centered at 1453.4 and 1317.6, the value expected for {(OEP)ReNCr(TTP)} + and {(OEP)-ReNCr(OEP)} + , respectively. Although other heterobimetallic µ-nitrido complexes have been reported, 16,17,[21][22][23] this is the first account of porphyrin containing complexes.…”
mentioning
confidence: 99%