Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/3290
Title: Hydrothermal synthesis of solid state materials and crystallography
Authors: Özmen, Bahar
Advisors: Eanes, Mehtap
Publisher: İzmir Institute of Technology
Izmir Institute of Technology
Abstract: The structure solution of the new polyoxovanadate compound([V16O31(OH)7]Cl· 15H2O), has been done by the SHELX crystal solution software. The compound was synthesized solvothermally at 170 0C in the Northwestern University. The compound crystallizes in the space group C2/c of the monoclinic system with eight formula units in a cell of dimensions a = 18.070 (2) Å, b = 17.414 (2) Å, c = 15.1154 (18) Å, â= 97.696 (2)°, V= 4713.8 (10) Å3 (T = 153 K). The structure is composed of vanadium-oxygen clusters encapsulating Cl¯ anion. Each of the V centers has square pyramidal geometry coordinated by five O atoms. The 16 (VO5) units are fused together through common edges to form (V16O38) cage with Cl¯ anion in the middle. The single crystals of the [Ni(en)3(VO3)2] compound was synthesized by hydrothermal method. [Ni(en)3(VO3)2] compound is in the crystal system of hexagonal and in the space group P61. The unit cell parameters are a = 8.9940 (13) Å, b = 8.9940 (13) Å, c = 34.001 (7) Å and á = 90 0, â = 90 0, ã = 120 0. The structure is composed of VO4 tetrahedras which are joined with others by sharing corners into infinite chains running along the c axis. The complex cation [Ni(en)3]2+ are located between the chains The chain in the compound has a repetitive sequence of 12-nuclear corner-sharing tetrahedras. The compound was synthesized at 160 0C for 3 days in the steel reaction autoclaves which have PTFE (Polytetrafluoroethylene) cups in them.
Description: Thesis (Master)--İzmir Institute of Technology, Chemistry, İzmir, 2004
Includes bibliographical references (leaves: 73)
Text in English; Abstract: Turkish and English
xii, 77 leaves
URI: http://hdl.handle.net/11147/3290
Appears in Collections:Master Degree / Yüksek Lisans Tezleri

Files in This Item:
File Description SizeFormat 
T000479.pdfMasterThesis3.4 MBAdobe PDFThumbnail
View/Open
Show full item record



CORE Recommender

Page view(s)

104
checked on Apr 22, 2024

Download(s)

60
checked on Apr 22, 2024

Google ScholarTM

Check





Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.