Abstract

Copper(II) carboxylate compounds with ethylamine and isopropylamine of the general formula [Cu2(RNH2)2(µ-O2CRf)4], where R = Et, iPr, and Rf = CnF2n+1, n = 1–6, were characterised in the condensed and gas phases by electron impact mass spectrometry (EI MS), IR spectroscopy, and thermal analysis. A mass spectra analysis confirmed the presence of metallated species in the gas phase. Among the observed fragments, the pseudomolecular ions [Cu2(RNH2)2(µ-O2CRf)3]+ were found, which suggests the dimeric structure of the studied complexes with axially N-coordinated ethyl- or isopropylamine molecules and bridging perfluorinated carboxylates. TGA studies demonstrated that copper transfer to the gas phase occurs even under atmospheric pressure. The temperature range of the [Cu2(RNH2)2(µ-O2CRf)4] and other copper carriers detection, observed in variable temperature infrared spectra, depends on the type of amine. The possible mechanisms of the decomposition of the tested compounds are proposed. The copper films were produced without additional reducing agents despite using Cu(II) CVD precursors in the chemical vapor deposition experiments. The layers of the gel-like complexes were fabricated in both spin- and dip-coating experiments, resulting in copper or copper oxide materials when heated. Dinuclear copper(II) carboxylate complexes with ethyl- and isopropylamine [Cu2(RNH2)2(µ-O2CRf)4] can be applied for the formation of metal or metal oxide materials, also in the nanoscale, by vapour and ‘wet’ deposition methods.

Highlights

  • Published: 4 December 2021Nowadays, copper compounds are applied as antifungal and antibacterial coatings, catalysts, or in the assembly of chemical and electrochemical sensors. [1]

  • In the case of other simple aliphatic amines, the following reaction: 2 [Cu(μ-O2 CRf )2 ] + 2 RNCO + 2H2 O → [Cu2 (RNH2 )2 (μ-O2 CRf )4 ] + 2CO2 is analogous to those we reported copper compounds containing tert-butylamine [9], as well as ethylamine [Cu2 (EtNH2 )2 (μ-O2 CC2 F5 )4 ] (2) and [Cu2 (EtNH2 )2 (μ-O2 CC3 F7 )4 ] (3) complexes [11,12]

  • Copper(II) carboxylate complexes group with ethylamine and isopropylamine of the general formula [Cu2 (RNH2 )2 (μ-O2 CRf )4 ] (1–10), where R = Et, i Pr, Rf = Cn F2n+1, n = 1–6, were synthesized in the reaction of copper(II) perfluorinated carboxylates with amines in situ generated from ethyl or isopropyl isocyanate

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Summary

Introduction

Copper compounds are applied as antifungal and antibacterial coatings, catalysts, or in the assembly of chemical and electrochemical sensors. [1]. The possibility of tert-butylamine copper(II) carboxylate complexes formation by applying tert-butyl isocyanate was described in our previous paper [9]. In the case of copper compounds, ‘wet’ deposition methods are the most often used for the copper(II) oxide materials formation. They are applied as heterogenic catalysts, in electrochemical cells for the Li2 CuO2 preparation, as electrodes in photoelectrochemical. The ethanolic solution of the [Cu2 (H2 O) (μ-O2 CCH3 )4 ] complex in the presence of monoethanolamine (MEA) was used for the copper(II) oxide layer formation by the dip-coating method. Copper carboxylate compounds were used for the metallic copper layer formation by a dip-coating method.

Materials
Instrumentation
Chemical Vapour Deposition Parameters
Spin- and Dip-Coating Parameters
Results and Discussion
Infrared Spectra Analysis
Mass Spectra Analysis
Results of Thermal Analysis
Temperature Variable Infrared Spectroscopy
CVD Experiments
Summary CVD
SpinSpin- and Dip-Coating
Spin-Coated Materials
Dip-Coated Materials
22. TEM data ofofthe
Conclusions
Methods
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