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Room-temperature synthesis of the Bi5[GaCl4]3 salt from three different classes of ionic liquids
Applied Physical Chemistry, KTH Royal Institute of Technology, Stockholm, Sweden.
Applied Physical Chemistry, KTH Royal Institute of Technology, Stockholm, Sweden.
Applied Physical Chemistry, KTH Royal Institute of Technology, Stockholm, Sweden.
2012 (engelsk)Inngår i: Journal of cluster science, ISSN 1040-7278, E-ISSN 1572-8862, Vol. 24, nr 1, s. 157-164Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Following the development in the synthesis of subvalent cluster compounds, we report on the use of three different classes of room-temperature ionic liquids for the synthesis of the pentabismuth-tris(tetragallate) salt, Bi-5[GaCl4](3), characterized by X-ray diffraction. The Bi-5[GaCl4](3) salt was prepared by reduction of BiCl3 using gallium metal in ionic liquid reaction media containing a strong Lewis acid, GaCl3. The ionic liquids; trihexyltetradecyl phosphonium chloride [Th-Td-P+]Cl-, 1-dodecyl-3-methylimidazolium chloride [Dod-Me-Im(+)]Cl- and N-butyl-N-methylpyrrolidinium chloride [Bu-Me-Pyrr(+)]Cl- from three of the main classes of ionic liquids were used in synthesis. Reactions using ionic liquids composed of the trihexyltetradecyl phosphonium cation [Th-Td-P+] and the anions; tetrafluoroborate [BF4 (-)], bis(trifluoro-methyl sulfonyl) imide [(Tf)(2)N-] and hexafluorophosphate [PF6 (-)] were also investigated.

sted, utgiver, år, opplag, sider
Springer, 2012. Vol. 24, nr 1, s. 157-164
Emneord [en]
Bismuth, Polycation, Cluster compounds, Ionic liquids, X-ray diffraction
HSV kategori
Identifikatorer
URN: urn:nbn:se:umu:diva-216255DOI: 10.1007/s10876-012-0526-3ISI: 000314678500015Scopus ID: 2-s2.0-84873742307OAI: oai:DiVA.org:umu-216255DiVA, id: diva2:1810084
Tilgjengelig fra: 2023-11-06 Laget: 2023-11-06 Sist oppdatert: 2023-11-08bibliografisk kontrollert
Inngår i avhandling
1. Subvalent cluster compounds and synthesis in alternative reaction media
Åpne denne publikasjonen i ny fane eller vindu >>Subvalent cluster compounds and synthesis in alternative reaction media
2012 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

With the aim of finding alternative reaction media for the synthesis of subvalent main group and transition metal cluster compounds, traditionally made through solid state reactions or in superacidic media, different alternative reaction media have been explored in this work. Room-temperature ionic liquids are amongst the more unconventional reaction media used. The syntheses performed have been aimed at both anionic and cationic cluster and the main tools used for characterization have been different X-ray diffraction and spectroscopic techniques.

Selected ionic liquids have along with dichloromethane been shown to work as alternative reaction media for room temperature synthesis of the Bi5[GaCl4]3 salt. The salt containing the subvalent naked bismuth polycation Bi53+ was isolated from reduction reactions of BiCl3 in Ga/GaCl3-dichloromethane respectively Ga/GaCl3-ioinc liquid media. Three different classes of ionic liquids based on phosphonium-, imidazolium- and pyrrolidinium- salts have been used in synthesis. Homopolyatomic clusters from the lighter Group 15 element arsenic have also been studied. Solutions from the oxidative and reductive reaction routes of arsenic and AsCl3 in Lewis acidic toluene media were studied by EXAFS spectroscopy. The results were evaluated using molecular dynamics simulations of arsenic clusters. A discussion on how the calculated As4 cluster model relates to the experimental data resulted from this study.

In terms of homopolyatomic anionic clusters the [K+(2,2,2-crypt)]2Ge92- compound containing the naked Ge92- anionic cluster has been isolated. The crystallographic investigation of [K+(2,2,2-crypt)]2Ge92- shows Zintl cluster anion Ge92- to be tricapped trigonal-prismatic with a symmetry very close to D3h. A chemical bonding analysis reveals two local minima of D3h symmetry and the cluster interaction scheme to be based on highly delocalised bonding.

Ligand supported transition metal clusters from tungsten and palladium have also been prepared. Reduction of WCl6 in a reaction mixture of ionic liquid and co-solvent toluene resulted in tritungsten decachloride; W3Cl10(MeCN)3, being formed. Furthermore, palladium sandwich compounds; [Pd2(Ga2Cl7)(C7H8)2], [Pd2(GaCl4)(C9H12)2]∙C9H12 and [Pd2(Ga2Cl7)(C6H5Cl)2] have been prepared using GaCl3-arene reaction media.

sted, utgiver, år, opplag, sider
Stockholm: KTH Royal Institute of Technology, 2012. s. 72
Serie
Trita-CHE-Report, ISSN 1654-1081 ; 2012:64
HSV kategori
Forskningsprogram
oorganisk kemi
Identifikatorer
urn:nbn:se:umu:diva-216251 (URN)9789175015798 (ISBN)
Opponent
Veileder
Forskningsfinansiär
Swedish Research Council, B61416
Merknad

Two additional manuscripts included in thesis.

Tilgjengelig fra: 2023-11-08 Laget: 2023-11-06 Sist oppdatert: 2023-11-08bibliografisk kontrollert

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