ベンゼン benzene
WordNet
- a colorless liquid hydrocarbon; highly inflammable; carcinogenic; the simplest of the aromatic compounds (同)benzine, benzol
PrepTutorEJDIC
- ベンゼン(コールタールから採る無色の液体)
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2016/06/19 01:56:52」(JST)
[Wiki ja表示]
化学式:C6H6(モル質量: 78.112 g/mol)は、
- ベンゼン
- ベンズバレン
- ビシクロプロペニル(英語版)
- デュワーベンゼン
- フルベン
- プリズマン
- ラジアレン(英語版)
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[Wiki en表示]
The molecular formula C6H6 (molar mass: 78.11 g/mol) may refer to:
- Benzene
- Benzvalene
- Bicyclopropenyl
- Dewar benzene
- Fulvene
- Prismane
- [3]Radialene
- 3-Methylidenepent-1-en-4-yne
- Hexadiyne
- 1,3-Hexadiyne
- 1,4-Hexadiyne
- 1,5-Hexadiyne
- 2,4-Hexadiyne
- Hexadienyne
- 1,2-Hexadien-4-yne
- 1,2-Hexadien-5-yne
- 1,3-Hexadien-5-yne
- 1,5-Hexadien-3-yne (divinylacetylene)
- 2,3-Hexadien-5-yne
English Journal
- Switching properties of Li-benzene complexes in a uniform electric field: a case where a "small" change makes a big difference.
- Sadlej-Sosnowska N1.
- Physical chemistry chemical physics : PCCP.Phys Chem Chem Phys.2015 Oct 7;17(37):23716-9. doi: 10.1039/c5cp03032c. Epub 2015 Aug 28.
- The effect of a homogeneous static electric field on the Li-benzene complex in two configurations, one with a larger Li-C6H6 distance ("loose") and one with a shorter distance ("tight"), has been investigated. The electric field has the same orientation as the direction of the dipole moments of the
- PMID 26315135
- Lewis Acidity of Si6Cl12 and Its Role as Convenient SiCl2 Source.
- Tillmann J1, Moxter M1, Bolte M1, Lerner HW1, Wagner M1.
- Inorganic chemistry.Inorg Chem.2015 Sep 17. [Epub ahead of print]
- The free cyclohexasilane Si6Cl12 (1) was obtained in 66% yield from the corresponding Cl- diadduct [nBu4N]2[1·2Cl] and AlCl3 in C6H6. The substituted cyclohexasilane 1,1-(Cl3Si)2Si6Cl10 (2), however, cannot be liberated from [nBu4N]2[2·2Cl] under comparable reaction conditions. Instead, a mixture
- PMID 26378930
- Scope and Mechanistic Analysis for Chemoselective Hydrogenolysis of Carbonyl Compounds Catalyzed by a Cationic Ruthenium Hydride Complex with a Tunable Phenol Ligand.
- Kalutharage N1, Yi CS1.
- Journal of the American Chemical Society.J Am Chem Soc.2015 Sep 2;137(34):11105-14. doi: 10.1021/jacs.5b06097. Epub 2015 Aug 25.
- A cationic ruthenium hydride complex, [(C6H6)(PCy3)(CO)RuH](+)BF4(-) (1), with a phenol ligand was found to exhibit high catalytic activity for the hydrogenolysis of carbonyl compounds to yield the corresponding aliphatic products. The catalytic method showed exceptionally high chemoselectivity towa
- PMID 26235841
Japanese Journal
- REACTION BEHAVIOR OF C₆H₆ IN THE THREE-WAY CATALYTIC CONVERTER EQUIPPED A GASOLINE ENGINE
- Takigawa Akio,Mieda Akihiro,Peng Yongzhen
- International journal of GEOMATE : geotechnique, construction materials and environment 6(1・2), 859-863, 2014-03
- NAID 40020102396
- Quenching Effect, Signal to Noise, Contrast to Noise Ratios on Scintillator Screens for Proton Beam Dosimetry System
- Kim Seonkyu,Lee Se Byeong,Yoo Seung Hoon [他],Cho Sungkoo,Kim Dong Wook,Shin Dongho,Park Sung Yong,Kim Chan Hyeong,Lee Sang Hoon
- Jpn J Appl Phys 51(4), 046401-046401-8, 2012-04-25
- … For comparison of the dosimetric properties, the quenching correction factors and standard deviations for the scintillator screens (C6H6, Gd2O2S:Tb, and Gd2O2S) were obtained using the relation between the light yield (scintillator-relative output) and the dose distribution (diode-relative output). … The SNRs of the scintillator screens (C6H6, Gd2O2S:Tb, and Gd2O2S) averaged 28.67, 40.18, and 24.56, respectively, at all ranges. …
- NAID 150000104492
- Pathways and Kinetics of Anisole Pyrolysis Studied by NMR and Selective ¹³C Labeling : Heterolytic Carbon Monoxide Generation
- Tsujino Yasuo,Yasaka Yoshiro,Matubayasi Nobuyuki [他],Nakahara Masaru
- Bulletin of the Chemical Society of Japan 85(1), 124-132, 2012-01-15
- … was converted to benzene, [12]C6H6 and phenol, [12]C6H5OH without ring disintegration. … The pyrolysis consists of two elementary steps: (1) the rate-determining unimolecular ether-bond fission (k1) to generate the fragmented product C6H6 and energized intermediate H[13]CHO* through the intramolecular proton transfer from the methoxy group to the phenyl, and (2) the fast bimolecular disproportionation (k2) through the intermolecular proton/hydride transfer from H[13]CHO* to H3[13]COC6H5 to produce [13]CO, [13]CH4, and C6H5OH. …
- NAID 10030217965
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★リンクテーブル★
[★]
ベンゼン
- 関
- benzole、C6H6
[★]
補体成分
- 同
- 補体第六成分 sixth component of complement
- 関
- 補体
脊椎
- 同
- 第6頚椎、第6頚椎、