The polarisability potential as a steric index
| dc.citation.epage | 959 | en_US |
| dc.citation.issue | 10 | en_US |
| dc.citation.spage | 955 | en_US |
| dc.citation.volume | 23 | en_US |
| dc.contributor.author | Camacho, Cristopher | en_US |
| dc.contributor.author | Mata-Segreda, Julio F. | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | 應用化學系分子科學碩博班 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.contributor.department | Institute of Molecular science | en_US |
| dc.date.accessioned | 2014-12-08T15:09:12Z | |
| dc.date.available | 2014-12-08T15:09:12Z | |
| dc.date.issued | 2010-10-01 | en_US |
| dc.description.abstract | The acid-catalysed hydrolysis of carboxylic esters is the reference chemical reaction used for the empirical evaluation of steric effects. In this work, the polarisability potential (Hehre, et al., J. Am. Chem. Soc. 1986, 108, 1711-1712) is identified as quantum-mechanical size of substituent groups. Correlation is found between this quantity and reactivity features of the reference reaction. Copyright (C) 2010 John Wiley & Sons, Ltd. | en_US |
| dc.identifier.doi | 10.1002/poc.1742 | en_US |
| dc.identifier.issn | 0894-3230 | en_US |
| dc.identifier.journal | JOURNAL OF PHYSICAL ORGANIC CHEMISTRY | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1002/poc.1742 | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/7012 | |
| dc.identifier.wosnumber | WOS:000283338800012 | |
| dc.language.iso | en_US | en_US |
| dc.subject | acid-catalysed ester hydrolysis | en_US |
| dc.subject | moment of inertia | en_US |
| dc.subject | polarisability potential | en_US |
| dc.subject | steric effect | en_US |
| dc.subject | Taft parameter | en_US |
| dc.subject | torsional barrier | en_US |
| dc.title | The polarisability potential as a steric index | en_US |
| dc.type | Article; Proceedings Paper | en_US |