Lucia Trevisan, Andrew D. Bond and Christopher A. Hunter
{"title":"羟基氢键网络中相互作用几何与协同性的关系","authors":"Lucia Trevisan, Andrew D. Bond and Christopher A. Hunter","doi":"10.1039/D5SC00784D","DOIUrl":null,"url":null,"abstract":"<p >Cooperativity between interactions in H-bonded networks can increase the strengths of H-bonds involving hydroxyl groups by up to 50%. The effect of changing the geometry of an intramolecular hydroxyl–hydroxyl H-bond on cooperativity with an intermolecular hydroxyl·quinuclidine H-bond was quantified by comparing the H-bonding properties of a series of hydroxycresols with the corresponding series of bisphenols. In the hydroxycresols, the intramolecular H-bond forms a 6-membered ring, and X-ray crystallography showed that the H-bond is distorted away from the ideal linear O–H⋯O geometry by up to 35°. In the bisphenols, the intramolecular H-bond forms an 8-membered ring, and the geometry is close to ideal, with the OH bond of the donor pointing directly at the lone pair of the acceptor. The presence of the intramolecular H-bonding interactions in solution was confirmed using <small><sup>1</sup></small>H NMR spectroscopy, and NMR titrations were used to measure the association constants for formation 1 : 1 complexes with quinuclidine in <em>n</em>-octane. Compared with the non-cooperative H-bond formed by benzyl alcohol with quinuclidine, the strength of the intermolecular H-bond formed by the hydroxycresols increased by between −8 kJ mol<small><sup>−1</sup></small> and −14 kJ mol<small><sup>−1</sup></small>, depending on the substituent <em>para</em> to the phenol OH donor. Electron-withdrawing substituents make the phenol a better H-bond donor, and the increase in the strength of the intramolecular H-bond leads to an increase in the strength of the intermolecular H-bond with quinuclidine. For the bisphenols, the cooperative effects were very similar: the substituent effects were practically identical, and the presence of the intramolecular H-bond increased the strength of the intermolecular interaction by between −10 kJ mol<small><sup>−1</sup></small> and −16 kJ mol<small><sup>−1</sup></small>. The results show that cooperativity in H-bonded networks depends strongly on the polarity of the interacting groups but is relatively insensitive to the precise geometric arrangement.</p>","PeriodicalId":9909,"journal":{"name":"Chemical Science","volume":" 17","pages":" 7418-7423"},"PeriodicalIF":7.4000,"publicationDate":"2025-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/sc/d5sc00784d?page=search","citationCount":"0","resultStr":"{\"title\":\"Relationship between interaction geometry and cooperativity measured in H-bonded networks of hydroxyl groups†\",\"authors\":\"Lucia Trevisan, Andrew D. Bond and Christopher A. Hunter\",\"doi\":\"10.1039/D5SC00784D\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Cooperativity between interactions in H-bonded networks can increase the strengths of H-bonds involving hydroxyl groups by up to 50%. The effect of changing the geometry of an intramolecular hydroxyl–hydroxyl H-bond on cooperativity with an intermolecular hydroxyl·quinuclidine H-bond was quantified by comparing the H-bonding properties of a series of hydroxycresols with the corresponding series of bisphenols. In the hydroxycresols, the intramolecular H-bond forms a 6-membered ring, and X-ray crystallography showed that the H-bond is distorted away from the ideal linear O–H⋯O geometry by up to 35°. In the bisphenols, the intramolecular H-bond forms an 8-membered ring, and the geometry is close to ideal, with the OH bond of the donor pointing directly at the lone pair of the acceptor. The presence of the intramolecular H-bonding interactions in solution was confirmed using <small><sup>1</sup></small>H NMR spectroscopy, and NMR titrations were used to measure the association constants for formation 1 : 1 complexes with quinuclidine in <em>n</em>-octane. Compared with the non-cooperative H-bond formed by benzyl alcohol with quinuclidine, the strength of the intermolecular H-bond formed by the hydroxycresols increased by between −8 kJ mol<small><sup>−1</sup></small> and −14 kJ mol<small><sup>−1</sup></small>, depending on the substituent <em>para</em> to the phenol OH donor. Electron-withdrawing substituents make the phenol a better H-bond donor, and the increase in the strength of the intramolecular H-bond leads to an increase in the strength of the intermolecular H-bond with quinuclidine. For the bisphenols, the cooperative effects were very similar: the substituent effects were practically identical, and the presence of the intramolecular H-bond increased the strength of the intermolecular interaction by between −10 kJ mol<small><sup>−1</sup></small> and −16 kJ mol<small><sup>−1</sup></small>. The results show that cooperativity in H-bonded networks depends strongly on the polarity of the interacting groups but is relatively insensitive to the precise geometric arrangement.</p>\",\"PeriodicalId\":9909,\"journal\":{\"name\":\"Chemical Science\",\"volume\":\" 17\",\"pages\":\" 7418-7423\"},\"PeriodicalIF\":7.4000,\"publicationDate\":\"2025-03-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2025/sc/d5sc00784d?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Science\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/sc/d5sc00784d\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Science","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/sc/d5sc00784d","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Relationship between interaction geometry and cooperativity measured in H-bonded networks of hydroxyl groups†
Cooperativity between interactions in H-bonded networks can increase the strengths of H-bonds involving hydroxyl groups by up to 50%. The effect of changing the geometry of an intramolecular hydroxyl–hydroxyl H-bond on cooperativity with an intermolecular hydroxyl·quinuclidine H-bond was quantified by comparing the H-bonding properties of a series of hydroxycresols with the corresponding series of bisphenols. In the hydroxycresols, the intramolecular H-bond forms a 6-membered ring, and X-ray crystallography showed that the H-bond is distorted away from the ideal linear O–H⋯O geometry by up to 35°. In the bisphenols, the intramolecular H-bond forms an 8-membered ring, and the geometry is close to ideal, with the OH bond of the donor pointing directly at the lone pair of the acceptor. The presence of the intramolecular H-bonding interactions in solution was confirmed using 1H NMR spectroscopy, and NMR titrations were used to measure the association constants for formation 1 : 1 complexes with quinuclidine in n-octane. Compared with the non-cooperative H-bond formed by benzyl alcohol with quinuclidine, the strength of the intermolecular H-bond formed by the hydroxycresols increased by between −8 kJ mol−1 and −14 kJ mol−1, depending on the substituent para to the phenol OH donor. Electron-withdrawing substituents make the phenol a better H-bond donor, and the increase in the strength of the intramolecular H-bond leads to an increase in the strength of the intermolecular H-bond with quinuclidine. For the bisphenols, the cooperative effects were very similar: the substituent effects were practically identical, and the presence of the intramolecular H-bond increased the strength of the intermolecular interaction by between −10 kJ mol−1 and −16 kJ mol−1. The results show that cooperativity in H-bonded networks depends strongly on the polarity of the interacting groups but is relatively insensitive to the precise geometric arrangement.
期刊介绍:
Chemical Science is a journal that encompasses various disciplines within the chemical sciences. Its scope includes publishing ground-breaking research with significant implications for its respective field, as well as appealing to a wider audience in related areas. To be considered for publication, articles must showcase innovative and original advances in their field of study and be presented in a manner that is understandable to scientists from diverse backgrounds. However, the journal generally does not publish highly specialized research.