Lanthanide shifts in the 1H N.M.R. spectra of peri-Alkoxy- and -Alkylamino-quinones

Donald W. Cameron; Geoffrey I. Feutrill; Antonio F. Patti

doi:10.1071/CH9771255

Lanthanide shifts in the ¹H N.M.R. spectra of peri-Alkoxy- and -Alkylamino-quinones

Donald W. Cameron
, Geoffrey I. Feutrill
, Antonio F. Patti

Research output: Contribution to journal › Article › Research › peer-review

7 Citations (Scopus)

Abstract

Unusually large lanthanide-induced shifts are observed for proton resonances of methoxy, ethoxy and dimethylamino substituents peri to carbonyl groups of anthraquinones and naphthoquinones. Such an arrangement allows the substrate to act as a bidentate ligand and is evidently the favoured site of coordination.

Original language	English
Pages (from-to)	1255-1258
Number of pages	4
Journal	Australian Journal of Chemistry
Volume	30
Issue number	6
DOIs	https://doi.org/10.1071/CH9771255
Publication status	Published - 1 Jan 1977
Externally published	Yes

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title = "Lanthanide shifts in the 1H N.M.R. spectra of peri-Alkoxy- and -Alkylamino-quinones",

abstract = "Unusually large lanthanide-induced shifts are observed for proton resonances of methoxy, ethoxy and dimethylamino substituents peri to carbonyl groups of anthraquinones and naphthoquinones. Such an arrangement allows the substrate to act as a bidentate ligand and is evidently the favoured site of coordination.",

author = "Cameron, \{Donald W.\} and Feutrill, \{Geoffrey I.\} and Patti, \{Antonio F.\}",

year = "1977",

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T1 - Lanthanide shifts in the 1H N.M.R. spectra of peri-Alkoxy- and -Alkylamino-quinones

AU - Cameron, Donald W.

AU - Feutrill, Geoffrey I.

AU - Patti, Antonio F.

PY - 1977/1/1

Y1 - 1977/1/1

N2 - Unusually large lanthanide-induced shifts are observed for proton resonances of methoxy, ethoxy and dimethylamino substituents peri to carbonyl groups of anthraquinones and naphthoquinones. Such an arrangement allows the substrate to act as a bidentate ligand and is evidently the favoured site of coordination.

AB - Unusually large lanthanide-induced shifts are observed for proton resonances of methoxy, ethoxy and dimethylamino substituents peri to carbonyl groups of anthraquinones and naphthoquinones. Such an arrangement allows the substrate to act as a bidentate ligand and is evidently the favoured site of coordination.

UR - https://www.scopus.com/pages/publications/84971061925

U2 - 10.1071/CH9771255

DO - 10.1071/CH9771255

M3 - Article

AN - SCOPUS:84971061925

SN - 0004-9425

VL - 30

SP - 1255

EP - 1258

JO - Australian Journal of Chemistry

JF - Australian Journal of Chemistry

IS - 6

ER -

Lanthanide shifts in the 1H N.M.R. spectra of peri-Alkoxy- and -Alkylamino-quinones

Abstract

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Lanthanide shifts in the ¹H N.M.R. spectra of peri-Alkoxy- and -Alkylamino-quinones