{"title":"混沌效应或疏水效应:纳米离子与非离子聚合物的独特结合特征","authors":"Max, Hohenschutz, Carlos Gonzalez, Lopez, Jasmin, Simons, Hannes, Luhmann, Martin, Dulle","doi":"10.26434/chemrxiv-2024-hkjpk","DOIUrl":null,"url":null,"abstract":"The nanometric ions (nano-ions) SiW12O404- (SiW) and B(C6H5)4- (BPh4) are considered as a superchaotropic and a hydro-phobic ion, respectively, in extension to the chaotropic side of the Hofmeister series. A distinction between chaotropic, superchaotropic and hydrophobic ions, however, has not been presented so far. Herein, we show by measurement of the viscosity B-coefficient of SiW (and other nano-ions) and of ion binding to the non-ionic polymer hydroxypropylcellulose (HPC), how chaotropic, superchaotropic and hydrophobic ions can be unambiguously distinguished. The viscosity B-coefficient of the superchaotropic SiW is positive as for hydrophobic ions, and distinct from classical chaotropic ions with a negative B-coefficient. In HPC-solution, BPh4 and SiW bind to the polymer, dramatically increasing the viscosity and the cloud point. Heating induces characteristically distinct responses for the two nano-ions: The viscosity rises for BPh4 and decreases for SiW. These effects are related to nano-ion induced aggregation and electric charging of HPC, which, upon heating, become stronger for BPh4 and weaker for SiW as shown by Small Angle X-ray and Neutron Scattering. 1H-Nuclear Magnetic Resonance and Isothermal Titration Calorimetry showed that the structural effects are linked to binding thermodynamics. Upon heating, the binding constant decreases for SiW and increases for BPh4 arising respectively from an enthalpically favorable, exothermic, chaotropic driving force or an enthalpically unfavorable, endothermic, hydropho-bic driving force. Combining the viscosity B-coefficient and sign of the binding enthalpy enables distinguishing cha-otropic, superchaotropic and hydrophobic ions. Importantly, superchaotropic binding can be stronger or weaker than hydrophobic binding depending on the temperature. Ion hydration and binding are demonstrated as powerful tools to tune polymer solution properties.","PeriodicalId":9813,"journal":{"name":"ChemRxiv","volume":"100 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Chaotropic or Hydrophobic Effect: Distinct binding signatures of nano-ions to a non-ionic polymer\",\"authors\":\"Max, Hohenschutz, Carlos Gonzalez, Lopez, Jasmin, Simons, Hannes, Luhmann, Martin, Dulle\",\"doi\":\"10.26434/chemrxiv-2024-hkjpk\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The nanometric ions (nano-ions) SiW12O404- (SiW) and B(C6H5)4- (BPh4) are considered as a superchaotropic and a hydro-phobic ion, respectively, in extension to the chaotropic side of the Hofmeister series. A distinction between chaotropic, superchaotropic and hydrophobic ions, however, has not been presented so far. Herein, we show by measurement of the viscosity B-coefficient of SiW (and other nano-ions) and of ion binding to the non-ionic polymer hydroxypropylcellulose (HPC), how chaotropic, superchaotropic and hydrophobic ions can be unambiguously distinguished. The viscosity B-coefficient of the superchaotropic SiW is positive as for hydrophobic ions, and distinct from classical chaotropic ions with a negative B-coefficient. In HPC-solution, BPh4 and SiW bind to the polymer, dramatically increasing the viscosity and the cloud point. Heating induces characteristically distinct responses for the two nano-ions: The viscosity rises for BPh4 and decreases for SiW. These effects are related to nano-ion induced aggregation and electric charging of HPC, which, upon heating, become stronger for BPh4 and weaker for SiW as shown by Small Angle X-ray and Neutron Scattering. 1H-Nuclear Magnetic Resonance and Isothermal Titration Calorimetry showed that the structural effects are linked to binding thermodynamics. Upon heating, the binding constant decreases for SiW and increases for BPh4 arising respectively from an enthalpically favorable, exothermic, chaotropic driving force or an enthalpically unfavorable, endothermic, hydropho-bic driving force. Combining the viscosity B-coefficient and sign of the binding enthalpy enables distinguishing cha-otropic, superchaotropic and hydrophobic ions. Importantly, superchaotropic binding can be stronger or weaker than hydrophobic binding depending on the temperature. Ion hydration and binding are demonstrated as powerful tools to tune polymer solution properties.\",\"PeriodicalId\":9813,\"journal\":{\"name\":\"ChemRxiv\",\"volume\":\"100 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-12-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ChemRxiv\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.26434/chemrxiv-2024-hkjpk\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemRxiv","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26434/chemrxiv-2024-hkjpk","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
纳米离子 SiW12O404- (SiW) 和 B(C6H5)4- (BPh4) 分别被认为是超各向同性离子和疏水性离子,是霍夫迈斯特(Hofmeister)系列中各向同性离子的延伸。然而,迄今为止还没有人提出过混沌离子、超混沌离子和疏水离子之间的区别。在此,我们通过测量 SiW(和其他纳米离子)的粘度 B 系数以及离子与非离子聚合物羟丙基纤维素(HPC)的结合情况,展示了如何明确区分各向混沌离子、超各向混沌离子和疏水离子。与疏水离子一样,超各向同性 SiW 的粘度 B 系数为正,而传统的各向同性离子的粘度 B 系数为负。在 HPC 溶液中,BPh4 和 SiW 与聚合物结合,大大增加了粘度和浊点。加热会导致两种纳米离子产生截然不同的反应:BPh4 的粘度上升,SiW 的粘度下降。小角 X 射线和中子散射显示,这些效应与纳米离子诱导的 HPC 聚合和电荷有关,加热后,BPh4 的聚合和电荷变得更强,而 SiW 的聚合和电荷变得更弱。1H-核磁共振和等温滴定量热法表明,结构效应与结合热力学有关。加热时,SiW 的结合常数会降低,而 BPh4 的结合常数会升高,这分别是由于焓有利、放热、混沌驱动力或焓不利、内热、亲水驱动力造成的。结合粘度 B 系数和结合焓的符号,可以区分混沌各向同性离子、超混沌各向同性离子和疏水离子。重要的是,超各向同性结合可能比疏水结合强,也可能比疏水结合弱,这取决于温度。离子水合和结合被证明是调整聚合物溶液特性的有力工具。
Chaotropic or Hydrophobic Effect: Distinct binding signatures of nano-ions to a non-ionic polymer
The nanometric ions (nano-ions) SiW12O404- (SiW) and B(C6H5)4- (BPh4) are considered as a superchaotropic and a hydro-phobic ion, respectively, in extension to the chaotropic side of the Hofmeister series. A distinction between chaotropic, superchaotropic and hydrophobic ions, however, has not been presented so far. Herein, we show by measurement of the viscosity B-coefficient of SiW (and other nano-ions) and of ion binding to the non-ionic polymer hydroxypropylcellulose (HPC), how chaotropic, superchaotropic and hydrophobic ions can be unambiguously distinguished. The viscosity B-coefficient of the superchaotropic SiW is positive as for hydrophobic ions, and distinct from classical chaotropic ions with a negative B-coefficient. In HPC-solution, BPh4 and SiW bind to the polymer, dramatically increasing the viscosity and the cloud point. Heating induces characteristically distinct responses for the two nano-ions: The viscosity rises for BPh4 and decreases for SiW. These effects are related to nano-ion induced aggregation and electric charging of HPC, which, upon heating, become stronger for BPh4 and weaker for SiW as shown by Small Angle X-ray and Neutron Scattering. 1H-Nuclear Magnetic Resonance and Isothermal Titration Calorimetry showed that the structural effects are linked to binding thermodynamics. Upon heating, the binding constant decreases for SiW and increases for BPh4 arising respectively from an enthalpically favorable, exothermic, chaotropic driving force or an enthalpically unfavorable, endothermic, hydropho-bic driving force. Combining the viscosity B-coefficient and sign of the binding enthalpy enables distinguishing cha-otropic, superchaotropic and hydrophobic ions. Importantly, superchaotropic binding can be stronger or weaker than hydrophobic binding depending on the temperature. Ion hydration and binding are demonstrated as powerful tools to tune polymer solution properties.