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・ Tetraethylammonium
・ Tetraethylammonium bromide
・ Tetraethylammonium chloride
・ Tetraethylammonium iodide
・ Tetraethylene glycol dimethyl ether
・ Tetraethylgermanium
・ Tetraethyllead
・ Tetraethylmethane
・ Tetraethyltin
・ Tetrafluoride
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・ Tetrafluoroberyllate
・ Tetrafluoroborate
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Tetrafluoromethane
・ Tetrafluorophenyl esters
・ Tetrafluoropropene
・ Tetrafluoropropylene
・ Tetrafucol A
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・ Tetragenococcus muriaticus
・ Tetragimyia
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・ Tetraglenes annamensis


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Tetrafluoromethane : ウィキペディア英語版
Tetrafluoromethane

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Tetrafluoromethane, also known as carbon tetrafluoride, is the simplest fluorocarbon (CF4). It has a very high bond strength due to the nature of the carbon–fluorine bond. It can also be classified as a haloalkane or halomethane. Because of the multiple carbon–fluorine bonds, and the highest electronegativity of fluorine, the carbon in tetrafluoromethane has a significant positive partial charge which strengthens and shortens the four carbon–fluorine bonds by providing additional ionic character. Tetrafluoromethane is a potent greenhouse gas.
==Bonding==
Carbon–fluorine bonds are the strongest in organic chemistry. Additionally, they strengthen as more carbon–fluorine bonds are added to the same carbon. In the one carbon organofluorine compounds represented by molecules of fluoromethane, difluoromethane, trifluoromethane, and tetrafluoromethane, the carbon–fluorine bonds are strongest in tetrafluoromethane. This effect is due to the increased coulombic attractions between the fluorine atoms and the carbon because the carbon has a positive partial charge of 0.76.〔

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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