کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1328916 1500080 2016 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
The role of inorganic acidity on templated vanadate composition and dimensionality
ترجمه فارسی عنوان
نقش اسیدیته معدنی بر ترکیب و ابعاد قالب بندی شده وانادات
کلمات کلیدی
رشد کریستال هیدروترمال قالب وانادات مکانیزم تشکیل تعاملات غیر کوانتومی
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
چکیده انگلیسی


• Analysis of hydrothermal crystal growth formation principles.
• Hydrothermal syntheses of organically templated vanadium phosphites and vanadium selenites.
• Non-covalent interaction index (NCI) calculations.

Compositional and structural differences in two organically templated vanadate compounds are directly ascribed to the acidity of the primary building units from which they are constructed. [C6H16N2][(VO)2(HPO3)3] and [C6H16N2][VO(SeO3)(HSeO3)]2 were synthesized under analogous conditions with either phosphorous or selenous acid. The acidities of these primary building units are reflected in both their relative protonation states and the compositions of the resulting solids. Differences in intermolecular interactions cause deviations in dimensionality of the resulting [(VO)2(HPO3)3]n2n−[(VO)2(HPO3)3]n2n− layers and [VO(SeO3)(HSeO3)]nn−[VO(SeO3)(HSeO3)]nn− chains, as identified and visualized using non-covalent interaction index calculations. Steric repulsions between adjacent [VO(SeO3)(HSeO3)]nn−[VO(SeO3)(HSeO3)]nn− chains preclude the formation of two-dimensional layers, such repulsions are absent in [C6H16N2][(VO)2(HPO3)3], as visualized using non-covalent interaction index calculations.

Differences in acidity between phosphorous and selenous acids cause marked differences in composition, structure and dimensionality between [C6H16N2][(VO)2(HPO3)3] and [C6H16N2][VO(SeO3)(HSeO3)]2, as visualized using non-covalent interaction index calculations.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Solid State Chemistry - Volume 236, April 2016, Pages 215–221
نویسندگان
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