一些d-金属离子与琥珀酸阴离子配位化合物在水-乙醇溶剂中的稳定性

N. V. Tukumova, T. R. Usacheva, Tran Thi Dieu Thuan, V. Sharnin, C. Giancola
{"title":"一些d-金属离子与琥珀酸阴离子配位化合物在水-乙醇溶剂中的稳定性","authors":"N. V. Tukumova, T. R. Usacheva, Tran Thi Dieu Thuan, V. Sharnin, C. Giancola","doi":"10.6060/ivkkt20186109-10.5778","DOIUrl":null,"url":null,"abstract":"The paper provides an overview of own data on complexation of nickel (II), cobalt (II) and cooper (II) ions with succinic acid anion in water-organic mixed solvents. Proper data are compared with data reported in literature for d-metal complexes with anions of maleic and succinic acids. The effect of aqueous ethanol solvent compositions on the stability of coordination compounds of M2+ with succinic acid anion as well as on рК values of stepwise succinic acid dissociation was carried out by a potentiometric titration at ionic strength of 0.1 maintained with sodium perchlorate at 298.15 ± 0.10 K. Mono ligand complexes of Ni2+, Co2+ and Cu2+ ions with succinic acid anion become stronger when ethanol content rises. In aqueous solutions Cu2+ ion forms stronger complexes with succinic and maleic acid anions than Ni2+ and Co2+ ions. In the studied water - ethanol solution this ratio is maintained for complexes with succinic acid anion, but a water-isopropanol solvent exerts leveling effect on the stability of complexes of nickel (II) and cobalt (II). An increase in the stability of complexes of d-metal with anions of maleic and succinic acids is due to the destabilization of the ligand with increasing ethanol concentration. The principal contribution of the changes in the solvation state of ligand is a typical for the stability changes of d-metal complexes with amine, glycinate, and acetate type ligands in water-organic mixed solvents. \nFor citation: \nTukumova N.V., Usacheva T.R., Thuan Tran Thi Dieu, Sharnin V.A., Giancola C. Stability of coordination compounds of some d-metal ions with succinic acid anion in aqueous-ethanol solvents. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol. 2018. V. 61. N 9-10. P. 15-22 \n ","PeriodicalId":45993,"journal":{"name":"Izvestiya Vysshikh Uchebnykh Zavedenii Khimiya i Khimicheskaya Tekhnologiya","volume":null,"pages":null},"PeriodicalIF":0.6000,"publicationDate":"2018-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"STABILITY OF COORDINATION COMPOUNDS OF SOME d-METAL IONS WITH SUCCINIC ACID ANION IN AQUEOUS-ETHANOL SOLVENTS\",\"authors\":\"N. V. Tukumova, T. R. Usacheva, Tran Thi Dieu Thuan, V. Sharnin, C. Giancola\",\"doi\":\"10.6060/ivkkt20186109-10.5778\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The paper provides an overview of own data on complexation of nickel (II), cobalt (II) and cooper (II) ions with succinic acid anion in water-organic mixed solvents. Proper data are compared with data reported in literature for d-metal complexes with anions of maleic and succinic acids. The effect of aqueous ethanol solvent compositions on the stability of coordination compounds of M2+ with succinic acid anion as well as on рК values of stepwise succinic acid dissociation was carried out by a potentiometric titration at ionic strength of 0.1 maintained with sodium perchlorate at 298.15 ± 0.10 K. Mono ligand complexes of Ni2+, Co2+ and Cu2+ ions with succinic acid anion become stronger when ethanol content rises. In aqueous solutions Cu2+ ion forms stronger complexes with succinic and maleic acid anions than Ni2+ and Co2+ ions. In the studied water - ethanol solution this ratio is maintained for complexes with succinic acid anion, but a water-isopropanol solvent exerts leveling effect on the stability of complexes of nickel (II) and cobalt (II). An increase in the stability of complexes of d-metal with anions of maleic and succinic acids is due to the destabilization of the ligand with increasing ethanol concentration. The principal contribution of the changes in the solvation state of ligand is a typical for the stability changes of d-metal complexes with amine, glycinate, and acetate type ligands in water-organic mixed solvents. \\nFor citation: \\nTukumova N.V., Usacheva T.R., Thuan Tran Thi Dieu, Sharnin V.A., Giancola C. Stability of coordination compounds of some d-metal ions with succinic acid anion in aqueous-ethanol solvents. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol. 2018. V. 61. N 9-10. P. 15-22 \\n \",\"PeriodicalId\":45993,\"journal\":{\"name\":\"Izvestiya Vysshikh Uchebnykh Zavedenii Khimiya i Khimicheskaya Tekhnologiya\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.6000,\"publicationDate\":\"2018-10-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Izvestiya Vysshikh Uchebnykh Zavedenii Khimiya i Khimicheskaya Tekhnologiya\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.6060/ivkkt20186109-10.5778\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Izvestiya Vysshikh Uchebnykh Zavedenii Khimiya i Khimicheskaya Tekhnologiya","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.6060/ivkkt20186109-10.5778","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 1

摘要

本文综述了在水-有机混合溶剂中镍(II)、钴(II)和铜(II)离子与琥珀酸阴离子的络合作用。将适当的数据与文献中报道的d-金属配合物与马来酸和琥珀酸阴离子的数据进行了比较。采用高氯酸钠在298.15±0.10 K下离子强度为0.1的电位滴定法,研究了乙醇水溶液组分对M2+与琥珀酸阴离子配合物稳定性和琥珀酸逐步解离рК值的影响。随着乙醇含量的增加,Ni2+、Co2+和Cu2+离子与琥珀酸阴离子的单配体配合物变得更强。在水溶液中,Cu2+离子与琥珀酸和马来酸阴离子形成比Ni2+和Co2+离子更强的配合物。在研究的水-乙醇溶液中,与琥珀酸阴离子的配合物保持这一比例,但水-异丙醇溶剂对镍(II)和钴(II)配合物的稳定性起平衡作用。d-金属与马来酸和琥珀酸阴离子配合物的稳定性增加是由于配体随着乙醇浓度的增加而不稳定。配体溶剂化状态变化的主要贡献是典型的d-金属配合物与胺、甘氨酸和乙酸型配体在水-有机混合溶剂中的稳定性变化。引用本文:图库蒙瓦,乌舍切瓦,陈建军,陈建军,陈建军。d-金属离子与琥珀酸阴离子配合物在水-乙醇溶剂中的稳定性研究。Izv。Vyssh。Uchebn。Zaved。Khim。Khim。Tekhnol》2018。v . 61。N 9。第15 - 22页
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
STABILITY OF COORDINATION COMPOUNDS OF SOME d-METAL IONS WITH SUCCINIC ACID ANION IN AQUEOUS-ETHANOL SOLVENTS
The paper provides an overview of own data on complexation of nickel (II), cobalt (II) and cooper (II) ions with succinic acid anion in water-organic mixed solvents. Proper data are compared with data reported in literature for d-metal complexes with anions of maleic and succinic acids. The effect of aqueous ethanol solvent compositions on the stability of coordination compounds of M2+ with succinic acid anion as well as on рК values of stepwise succinic acid dissociation was carried out by a potentiometric titration at ionic strength of 0.1 maintained with sodium perchlorate at 298.15 ± 0.10 K. Mono ligand complexes of Ni2+, Co2+ and Cu2+ ions with succinic acid anion become stronger when ethanol content rises. In aqueous solutions Cu2+ ion forms stronger complexes with succinic and maleic acid anions than Ni2+ and Co2+ ions. In the studied water - ethanol solution this ratio is maintained for complexes with succinic acid anion, but a water-isopropanol solvent exerts leveling effect on the stability of complexes of nickel (II) and cobalt (II). An increase in the stability of complexes of d-metal with anions of maleic and succinic acids is due to the destabilization of the ligand with increasing ethanol concentration. The principal contribution of the changes in the solvation state of ligand is a typical for the stability changes of d-metal complexes with amine, glycinate, and acetate type ligands in water-organic mixed solvents. For citation: Tukumova N.V., Usacheva T.R., Thuan Tran Thi Dieu, Sharnin V.A., Giancola C. Stability of coordination compounds of some d-metal ions with succinic acid anion in aqueous-ethanol solvents. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol. 2018. V. 61. N 9-10. P. 15-22  
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
1.40
自引率
44.40%
发文量
83
期刊最新文献
Mathematical modeling of deformation and relaxation processes of polymer yarn Study of integration of software applications into design process The significance of VKHUTEMAS in the development of theatrical culture in Russia of XX-XXI centuries Method of measuring fibers’ friction bending resistance Study of physical and mechanical properties of knitted fabrics
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1