Ring inversion of CH2-X-CH2-bridged peri-naphthalenes. A dynamic n.m.r. study
Research output: Contribution to journal › Journal article › Research › peer-review
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.
Original language | English |
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Journal | Journal of the Chemical Society, Chemical Communications |
Issue number | 6 |
Pages (from-to) | 333-334 |
Number of pages | 2 |
ISSN | 0022-4936 |
DOIs | |
Publication status | Published - 1 Jan 1982 |
ID: 218714388