LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Tris Chelating Phosphate Complexes of Bis(thio)urea Ligands
DepartmentOSSO国家重点实验室
Li R(李瑞); Zhao YX(赵艳霞); Li SG(李少光); Yang PJ(杨培菊); Huang XJ(黄晓卷); Yang XJ(杨晓娟); Wu B(吴彪); Wu B(吴彪)
The second departmenterc国家工程研究中心
2013
Source PublicationInorganic Chemistry
ISSN0020-1669
Volume52Pages:5851-5860
AbstractTwo bisurea (L1, L2) and one bisthiourea (L3) ligands were synthesized and their anion coordination behavior was studied. These ligands can readily form the tris chelates [PO4(L)3]3 (1, 5, and 6) with phosphate ion (PO43) in the solid state, in which the anion is coordinated by six urea groups through 12 hydrogen bonds. Solution binding studies by 1H NMR and UV−vis spectroscopy revealed different binding properties of the ligands toward phosphate ion. While the bis(p-nitrophenyl)-substituted bisurea L1 retains the 3:1 (host to guest) binding ratio in solution, the diethyl derivative L2 only forms 1:1 complex with phosphate ion. The more acidic thiourea L3 undergoes deprotonation/decomposition in the presence of phosphate ion. Moreover, the sulfate complex (2) of L1 and bicarbonate (3) and carbonate (4) complexes of L2 have also been obtained, which show lower coordination numbers both in the solid state and in solution.
Subject Area物理化学与绿色催化
Funding Organizationthe National Natural Science Foundation of China (Grant 21271149)
Indexed BySCI
If4.794
Language英语
Funding Project金属有机功能材料研究组;日常管理与大型仪器组
compositor第一作者单位
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/4722
Collection羰基合成与选择氧化国家重点实验室(OSSO)
精细石油化工中间体国家工程研究中心(ERC)
Corresponding AuthorWu B(吴彪)
Recommended Citation
GB/T 7714
Li R,Zhao YX,Li SG,et al. Tris Chelating Phosphate Complexes of Bis(thio)urea Ligands[J]. Inorganic Chemistry,2013,52:5851-5860.
APA Li R.,Zhao YX.,Li SG.,Yang PJ.,Huang XJ.,...&吴彪.(2013).Tris Chelating Phosphate Complexes of Bis(thio)urea Ligands.Inorganic Chemistry,52,5851-5860.
MLA Li R,et al."Tris Chelating Phosphate Complexes of Bis(thio)urea Ligands".Inorganic Chemistry 52(2013):5851-5860.
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