1H and 13C n.m.r. study of butatriene‐bis‐tricarbonyliron complexes. Assignment of geometric orientation by comparative J(CCCH) values

Rae Victor; Israel Ringel

doi:10.1002/mrc.1270110108

¹H and ¹³C n.m.r. study of butatriene‐bis‐tricarbonyliron complexes. Assignment of geometric orientation by comparative J(CCCH) values

Rae Victor^*
, Israel Ringel

^*Corresponding author for this work

School of Pharmacy

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

7 Scopus citations

Abstract

A number of substituted butatriene‐bis‐tricarbonyliron complexes have been studied by ¹³C and ¹H n.m.r. spectroscopy. Long range coupling values, J(CCCH), have confirmed chemical shift results that methyl and phenyl groups assume opposite orientations at the coordinated double bonds with the methyl group preferentially trans to carbon and the phenyl group preferentially trans to iron.

Original language	English
Pages (from-to)	31-33
Number of pages	3
Journal	Organic Magnetic Resonance
Volume	11
Issue number	1
DOIs	https://doi.org/10.1002/mrc.1270110108
State	Published - Jan 1978

Access to Document

10.1002/mrc.1270110108

Cite this

@article{35716c6e7647421b80535b89af37098f,

title = "1H and 13C n.m.r. study of butatriene‐bis‐tricarbonyliron complexes. Assignment of geometric orientation by comparative J(CCCH) values",

abstract = "A number of substituted butatriene‐bis‐tricarbonyliron complexes have been studied by 13C and 1H n.m.r. spectroscopy. Long range coupling values, J(CCCH), have confirmed chemical shift results that methyl and phenyl groups assume opposite orientations at the coordinated double bonds with the methyl group preferentially trans to carbon and the phenyl group preferentially trans to iron.",

author = "Rae Victor and Israel Ringel",

year = "1978",

month = jan,

doi = "10.1002/mrc.1270110108",

language = "אנגלית",

volume = "11",

pages = "31--33",

journal = "Organic Magnetic Resonance",

issn = "0030-4921",

publisher = "John Wiley and Sons Ltd",

number = "1",

}

TY - JOUR

T1 - 1H and 13C n.m.r. study of butatriene‐bis‐tricarbonyliron complexes. Assignment of geometric orientation by comparative J(CCCH) values

AU - Victor, Rae

AU - Ringel, Israel

PY - 1978/1

Y1 - 1978/1

N2 - A number of substituted butatriene‐bis‐tricarbonyliron complexes have been studied by 13C and 1H n.m.r. spectroscopy. Long range coupling values, J(CCCH), have confirmed chemical shift results that methyl and phenyl groups assume opposite orientations at the coordinated double bonds with the methyl group preferentially trans to carbon and the phenyl group preferentially trans to iron.

AB - A number of substituted butatriene‐bis‐tricarbonyliron complexes have been studied by 13C and 1H n.m.r. spectroscopy. Long range coupling values, J(CCCH), have confirmed chemical shift results that methyl and phenyl groups assume opposite orientations at the coordinated double bonds with the methyl group preferentially trans to carbon and the phenyl group preferentially trans to iron.

UR - https://www.scopus.com/pages/publications/84913796977

U2 - 10.1002/mrc.1270110108

DO - 10.1002/mrc.1270110108

M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???

AN - SCOPUS:84913796977

SN - 0030-4921

VL - 11

SP - 31

EP - 33

JO - Organic Magnetic Resonance

JF - Organic Magnetic Resonance

IS - 1

ER -

¹H and ¹³C n.m.r. study of butatriene‐bis‐tricarbonyliron complexes. Assignment of geometric orientation by comparative J(CCCH) values

Abstract

Access to Document

Other files and links

Fingerprint

Cite this