Ring inversion of CH2-X-CH2-bridged peri-naphthalenes. A dynamic n.m.r. study

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Standard

Ring inversion of CH2-X-CH2-bridged peri-naphthalenes. A dynamic n.m.r. study. / Anderson, J. Edgar; Jørgensen, Flemming S.; Thomsen, Tove.

In: Journal of the Chemical Society, Chemical Communications, No. 6, 01.01.1982, p. 333-334.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Anderson, JE, Jørgensen, FS & Thomsen, T 1982, 'Ring inversion of CH2-X-CH2-bridged peri-naphthalenes. A dynamic n.m.r. study', Journal of the Chemical Society, Chemical Communications, no. 6, pp. 333-334. https://doi.org/10.1039/C39820000333

APA

Anderson, J. E., Jørgensen, F. S., & Thomsen, T. (1982). Ring inversion of CH2-X-CH2-bridged peri-naphthalenes. A dynamic n.m.r. study. Journal of the Chemical Society, Chemical Communications, (6), 333-334. https://doi.org/10.1039/C39820000333

Vancouver

Anderson JE, Jørgensen FS, Thomsen T. Ring inversion of CH2-X-CH2-bridged peri-naphthalenes. A dynamic n.m.r. study. Journal of the Chemical Society, Chemical Communications. 1982 Jan 1;(6):333-334. https://doi.org/10.1039/C39820000333

Author

Anderson, J. Edgar ; Jørgensen, Flemming S. ; Thomsen, Tove. / Ring inversion of CH2-X-CH2-bridged peri-naphthalenes. A dynamic n.m.r. study. In: Journal of the Chemical Society, Chemical Communications. 1982 ; No. 6. pp. 333-334.

Bibtex

@article{57917f7b4056481fb7f7644d77b98f57,
title = "Ring inversion of CH2-X-CH2-bridged peri-naphthalenes. A dynamic n.m.r. study",
abstract = "Barriers to the inversion of the six-membered rings formed by bridging the 1 - and 8-positions of naphthalene with a CH2-X-CH2 chain (X = 0,S,Se, or Te) increase along the series, O<S<Se<Te, in marked contrast with the corresponding pentamethylene heterocycles, reflecting the importance of bond angle strain during inversion.",
author = "Anderson, {J. Edgar} and J{\o}rgensen, {Flemming S.} and Tove Thomsen",
year = "1982",
month = jan,
day = "1",
doi = "10.1039/C39820000333",
language = "English",
pages = "333--334",
journal = "Journal of the Chemical Society D: Chemical Communications",
issn = "0577-6171",
publisher = "Royal Society of Chemistry",
number = "6",

}

RIS

TY - JOUR

T1 - Ring inversion of CH2-X-CH2-bridged peri-naphthalenes. A dynamic n.m.r. study

AU - Anderson, J. Edgar

AU - Jørgensen, Flemming S.

AU - Thomsen, Tove

PY - 1982/1/1

Y1 - 1982/1/1

N2 - Barriers to the inversion of the six-membered rings formed by bridging the 1 - and 8-positions of naphthalene with a CH2-X-CH2 chain (X = 0,S,Se, or Te) increase along the series, O<S<Se<Te, in marked contrast with the corresponding pentamethylene heterocycles, reflecting the importance of bond angle strain during inversion.

AB - Barriers to the inversion of the six-membered rings formed by bridging the 1 - and 8-positions of naphthalene with a CH2-X-CH2 chain (X = 0,S,Se, or Te) increase along the series, O<S<Se<Te, in marked contrast with the corresponding pentamethylene heterocycles, reflecting the importance of bond angle strain during inversion.

UR - http://www.scopus.com/inward/record.url?scp=37049097305&partnerID=8YFLogxK

U2 - 10.1039/C39820000333

DO - 10.1039/C39820000333

M3 - Journal article

AN - SCOPUS:37049097305

SP - 333

EP - 334

JO - Journal of the Chemical Society D: Chemical Communications

JF - Journal of the Chemical Society D: Chemical Communications

SN - 0577-6171

IS - 6

ER -

ID: 218714388