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Journal ArticleDOI

Synthesis and crystal structure of the double barium–titanium isopropoxide [Ba4Ti4(µ4-O)4(µ3-OR)2(µ-OR)8(OR)6(ROH)4][Ba4Ti4(µ4-O)4(µ3-OR)2(µ-OR)9(OR)5(ROH)3]

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TLDR
An X-ray structural study of the crystals isolated from the solutions obtained by the reaction of Ba metal with Ti(OPri)4 in isopropyl alcohol has been carried out; the crystals of the compound, which is a precursor for the synthesis of BaTiO3, contain molecules of two different kinds [Ba4Ti4O4(OR)16(ROH)4], where R = Pri as mentioned in this paper.
Abstract
An X-ray structural study of the crystals isolated from the solutions obtained by the reaction of Ba metal with Ti(OPri)4 in isopropyl alcohol has been carried out; the crystals of the compound, which is a precursor for the synthesis of BaTiO3, contain molecules of two different kinds [Ba4Ti4O4(OR)16(ROH)4] and [Ba4Ti4O4(OR)16(ROH)3], where R = Pri.

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Citations
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Structure, photochemistry and applications of metal-doped polyoxotitanium alkoxide cages.

TL;DR: The structural trends in M-POTs, their electronic behaviour and their applications as single-source precursors are highlighted, looking at current and future trends in the development of inorganic precursor for device applications.
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Volatile metallo-organic precursors for depositing inorganic electronic materials

TL;DR: In this paper, the authors present a method of photolytic decomposition of metallo-organic molecular precursors for chemical vapour deposition (MOCVD) under UHV conditions.
Journal ArticleDOI

Precursor directed synthesis – “molecular” mechanisms in the Soft Chemistry approaches and their use for template-free synthesis of metal, metal oxide and metal chalcogenide nanoparticles and nanostructures

TL;DR: This review provides an insight into the common reaction mechanisms in Soft Chemistry processes involved in nucleation, growth and aggregation of metal, metal oxide and chalcogenide nanoparticles starting from metal-organic precursors and demonstrates how mastering the precursor chemistry permits us to control the chemical and phase composition, crystallinity, morphology, porosity and surface characteristics of produced nanomaterials.
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The chemistry behind the sol–gel synthesis of complex oxide nanoparticles for bio-imaging applications

TL;DR: In this paper, the formation of nanoparticles in hydrolytic and non-hydrolytic reactions in organic media is treated as a borderline case of coordination chemistry equilibria.
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Precursor and solvent effects in the nonhydrolytic synthesis of complex oxide nanoparticles for bioimaging applications by the ether elimination (Bradley) reaction.

TL;DR: Investigation of the solvent and alkoxide precursor effect on the nonhydrolytic sol-gel synthesis of oxide nanoparticles by means of an ether elimination (Bradley) reaction indicates that the best crystallinity of the resulting oxide particles is achieved on application of aprotic ketone solvents and of smallest possible alkoxide groups.
References
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Journal ArticleDOI

Preparation of High-Purity Submicron Barium Titanate Powders

TL;DR: Simultaneous hydrolytic decomposition of barium bis isopropoxide and titanium tetrakis tertiary amyloxide was used to produce stoichiometric BaTiO3.
Journal ArticleDOI

Preparation and Characterization of Alkoxy-Derived SrZrO3 and SrTiO3

TL;DR: In this article, high-purity strontium, zirconium, and titanium alkoxides were synthesized and characterized as precursors for complex oxides.
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Alkoxide synthesis techniques for BaTiO3

TL;DR: Several variations of the sol-gel process leading to polycrystalline BaTiO3 formation were explored and compared in this article, leading to the discovery of barium-titanium isopropoxide single crystals with a fixed Ba:Ti stoichiometry of [1:1].
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The Crystal and Molecular Structure of Dichlorodiphenoxytitanium(IV)

TL;DR: X-ray crystal structural analysis of tetraethyl titanates and monomethyltriethyl titanate, determining reason for difference in color was carried out in this paper, showing that the difference in colour can be attributed to the properties of the crystal lattice.
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