Litium karbida
Litium karbida, Li2C2, sering dikenal sebagai dilitium asetilida , adalah senyawa kimia dari litium dan karbon, suatu asetilida. Ia merupakan senyawa antara yang dihasilkan selama prosedur penanggalan radiokarbon. Li2C2 adalah salah satu dari serangkaian senyawa litium-karbon yang meliputi senyawa kaya litium: Li4C, Li6C2, Li8C3, Li6C3, Li4C3, Li4C5, dan senyawa interkalasi grafit : LiC6, LiC12, dan LiC18.
Nama | |
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Nama IUPAC (preferensi)
Lithium carbide | |
Nama IUPAC (sistematis)
Dilithium(1+) ethyne | |
Nama lain
Dilitium asetilida
Litium dikarbon | |
Penanda | |
Model 3D (JSmol)
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3DMet | {{{3DMet}}} |
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PubChem CID
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Nomor RTECS | {{{value}}} |
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Sifat | |
Li2C2 | |
Massa molar | 37,9034 g/mol |
Densitas | 1,3 g/cm³[1] |
Titik lebur | > 550°C |
Kelarutan | tidak larut dalam pelarut organik |
Kecuali dinyatakan lain, data di atas berlaku pada suhu dan tekanan standar (25 °C [77 °F], 100 kPa). | |
verifikasi (apa ini ?) | |
Referensi | |
Li2C2 adalah senyawa kaya litium yang paling stabil secara termodinamika[2] dan satu-satunya yang dapat diperoleh langsung dari unsurnya. Ia pertama kali dibuat oleh Moissan, pada tahun 1896[3] yang mereaksikan arang dengan litium karbonat. Senyawa kaya litium lainnya dibuat dengan mereaksikan uap litium dengan hidrokarbon terklorinasi , misalnya CCl4.
Litium karbida kadang-kadang dibingungkan dengan obat litium karbonat, Li2O3, karena kemiripan namanya.
Preparation and chemistry
In the laboratory samples may be prepared by treating acetylene with a solution of lithium in ammonia.
- C2H2 + 2 Li → Li2C2 + H2
Samples prepared in this manner generally are poorly crystalline. Crystalline samples may be prepared by a reaction between molten lithium and graphite at over 1000 °C.[2] Li2C2 can also be prepared by reacting CO2 with molten lithium.
Lithium carbide is hydrolyses readily to form acetylene:
- C2Li2 + H2O → C2H2 + LiOH
Structure
Li2C2 is a Zintl phase compound and exists as a salt, 2Li+C22−. Its reactivity, combined with the difficulty in growing suitable single crystals, has made the determination of its crystal structure difficult. It adopts a distorted anti-fluorite crystal structure, similar to that of rubidium peroxide (Rb2O2) and caesium peroxide (Cs2O2). Each Li atom is surrounded by six carbon atoms from 4 different acetylides, with two acetylides co-ordinating side -on and the other two end-on.[2][4] The observed C-C distance of 120 pm indicates the presence of a C≡C triple bond. At high temperatures Li2C2 transforms reversibly to a cubic anti-fluorite structure.[5]
Use in radiocarbon dating
There are a number of procedures employed, some that burn the sample producing CO2 that is then reacted with lithium, and others where the carbon containing sample is reacted directly with lithium metal.[6] The outcome is the same: Li2C2 is produced, which can then be used to create species easy to mass, like acetylene and benzene.[7] Note that lithium nitride may be formed and this produces ammonia when hydrolyzed, which contaminates the acetylene gas.
References
- ^ R. Juza; V. Wehle; H.-U. Schuster (1967). "Zur Kenntnis des Lithiumacetylids". Zeitschrift für anorganische und allgemeine Chemie. 352 (5–6): 252. doi:10.1002/zaac.19673520506.
- ^ a b c Ruschewitz, Uwe (September 2003). "Binary and ternary carbides of alkali and alkaline-earth metals". Coordination Chemistry Reviews. 244 (1-2): 115–136. doi:10.1016/S0010-8545(03)00102-4.
- ^ H. Moissan Comptes Rendus hebd. Seances Acad. Sci. 122, 362 (1896)
- ^ Juza, Robert; Opp, Karl (November 1951). "Metallamide und Metallnitride, 24. Mitteilung. Die Kristallstruktur des Lithiumamides". Zeitschrift für anorganische und allgemeine Chemie (dalam bahasa German). 266 (6): 313–324. doi:10.1002/zaac.19512660606.
- ^ U. Ruschewitz; R. Pöttgen (1999). "Structural Phase Transition in Li2C2". Zeitschrift für anorganische und allgemeine Chemie. 625 (10): 1599–1603. doi:10.1002/(SICI)1521-3749(199910)625:10<1599::AID-ZAAC1599>3.0.CO;2-J.
- ^ Swart E.R. (1964). "The direct conversion of wood charcoal to lithium carbide in the production of acetylene for radiocarbon dating". Cellular and Molecular Life Sciences. 20: 47. doi:10.1007/BF02146038.
- ^ University of Zurich Radiocarbon Laboratory webpage