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Niobium(v) and tantalum(v) halide chalcogenoether complexes – towards single source CVD precursors for ME2thin films

Niobium(v) and tantalum(v) halide chalcogenoether complexes – towards single source CVD precursors for ME2thin films
Niobium(v) and tantalum(v) halide chalcogenoether complexes – towards single source CVD precursors for ME2thin films
A series of pentavalent niobium and tantalum halide complexes with thio-, seleno- and telluro-ether ligands, [MCl5(EnBu2)] (M = Nb, Ta; E = S, Se, Te), [TaX5(TeMe2)] (X = Cl, Br, F) and the dinuclear [(MCl5)2{o-C6H4(CH2SEt)2}] (M = Nb, Ta), has been prepared and characterised by IR, 1H, 13C{1H}, 77Se, 93Nb and 125Te NMR spectroscopy, as appropriate, and microanalyses. Confirmation of the tantalum(V)–telluroether coordination follows from the crystal structure of [TaCl5(TeMe2)], which represents the highest oxidation state transition metal complex with telluroether coordination structurally authenticated. The Ta(V) monotelluroether complexes are much more stable than the Nb(V) analogues. In the presence of TaCl5 the ditelluroether, CH2(CH2TetBu)2, is decomposed; one of the products is the dealkylated [tBuTe(CH2)3Te][TaCl6], whose structure was determined crystallographically. Crystal structures of [(MCl5)2{o-C6H4(CH2SEt)2}] (M = Nb, Ta) show ligand-bridged species. The complexes bearing ?-hydrogen atoms on the terminal alkyl substituents have also been investigated as single source reagents for the deposition of ME2 thin films via low pressure chemical vapour deposition. While the tantalum complexes proved to be unsuitable, the [NbCl5(SnBu2)] and [NbCl5(SenBu2)] deposit NbS2 and NbSe2 as hexagonal platelets onto SiO2 substrates at 750 °C and 650 °C, respectively. Grazing incidence and in-plane X-ray diffraction confirm both materials adopt the 3R-polytype (R3mh), and the sulfide shows preferred orientation with the crystallites aligned predominantly with the c axis perpendicular to the substrate. Scanning electron microscopy and Raman spectra are consistent with the X-ray data.
0300-9246
16640-16648
Benjamin, Sophie L.
3efd7555-c2e0-4330-a289-681bd13700df
Chang, Y.
e2c39dfe-7510-4f82-a929-e347c4bc85b3
Gurnani, Chitra
18063024-d052-4fe3-8a79-fdecd227bc2c
Hector, Andrew Lee
f19a8f31-b37f-4474-b32a-b7cf05b9f0e5
Huggon, M.
62bb438c-6a18-4758-831d-039958cf6a0d
Levason, William
e7f6d7c7-643c-49f5-8b57-0ebbe1bb52cd
Reid, Gillian
37d35b11-40ce-48c5-a68e-f6ce04cd4037
Benjamin, Sophie L.
3efd7555-c2e0-4330-a289-681bd13700df
Chang, Y.
e2c39dfe-7510-4f82-a929-e347c4bc85b3
Gurnani, Chitra
18063024-d052-4fe3-8a79-fdecd227bc2c
Hector, Andrew Lee
f19a8f31-b37f-4474-b32a-b7cf05b9f0e5
Huggon, M.
62bb438c-6a18-4758-831d-039958cf6a0d
Levason, William
e7f6d7c7-643c-49f5-8b57-0ebbe1bb52cd
Reid, Gillian
37d35b11-40ce-48c5-a68e-f6ce04cd4037

Benjamin, Sophie L., Chang, Y., Gurnani, Chitra, Hector, Andrew Lee, Huggon, M., Levason, William and Reid, Gillian (2014) Niobium(v) and tantalum(v) halide chalcogenoether complexes – towards single source CVD precursors for ME2thin films. Dalton Transactions, 43 (44), 16640-16648. (doi:10.1039/c4dt02694b).

Record type: Article

Abstract

A series of pentavalent niobium and tantalum halide complexes with thio-, seleno- and telluro-ether ligands, [MCl5(EnBu2)] (M = Nb, Ta; E = S, Se, Te), [TaX5(TeMe2)] (X = Cl, Br, F) and the dinuclear [(MCl5)2{o-C6H4(CH2SEt)2}] (M = Nb, Ta), has been prepared and characterised by IR, 1H, 13C{1H}, 77Se, 93Nb and 125Te NMR spectroscopy, as appropriate, and microanalyses. Confirmation of the tantalum(V)–telluroether coordination follows from the crystal structure of [TaCl5(TeMe2)], which represents the highest oxidation state transition metal complex with telluroether coordination structurally authenticated. The Ta(V) monotelluroether complexes are much more stable than the Nb(V) analogues. In the presence of TaCl5 the ditelluroether, CH2(CH2TetBu)2, is decomposed; one of the products is the dealkylated [tBuTe(CH2)3Te][TaCl6], whose structure was determined crystallographically. Crystal structures of [(MCl5)2{o-C6H4(CH2SEt)2}] (M = Nb, Ta) show ligand-bridged species. The complexes bearing ?-hydrogen atoms on the terminal alkyl substituents have also been investigated as single source reagents for the deposition of ME2 thin films via low pressure chemical vapour deposition. While the tantalum complexes proved to be unsuitable, the [NbCl5(SnBu2)] and [NbCl5(SenBu2)] deposit NbS2 and NbSe2 as hexagonal platelets onto SiO2 substrates at 750 °C and 650 °C, respectively. Grazing incidence and in-plane X-ray diffraction confirm both materials adopt the 3R-polytype (R3mh), and the sulfide shows preferred orientation with the crystallites aligned predominantly with the c axis perpendicular to the substrate. Scanning electron microscopy and Raman spectra are consistent with the X-ray data.

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Published date: 18 September 2014
Organisations: Electrochemistry

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Local EPrints ID: 373032
URI: http://eprints.soton.ac.uk/id/eprint/373032
ISSN: 0300-9246
PURE UUID: 4f6734af-d461-453c-a8c3-d177fbefef4e
ORCID for Andrew Lee Hector: ORCID iD orcid.org/0000-0002-9964-2163
ORCID for William Levason: ORCID iD orcid.org/0000-0003-3540-0971
ORCID for Gillian Reid: ORCID iD orcid.org/0000-0001-5349-3468

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Date deposited: 06 Jan 2015 12:10
Last modified: 15 Mar 2024 02:52

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Contributors

Author: Sophie L. Benjamin
Author: Y. Chang
Author: Chitra Gurnani
Author: M. Huggon
Author: William Levason ORCID iD
Author: Gillian Reid ORCID iD

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