Результаты поиска

| IUPACName = bis(2,3,4,5,6-pentafluorophenyl)xenon | ImageFile = Bis(pentafluorophenyl)xenon conformation.png ...

...doi=10.15227/orgsyn.059.0122}}</ref> Illustrative is preparation of [[tris(pentafluorophenyl)borane]]:<ref>Piers, W. E.; Chivers, T. “Pentafluorophenylboranes: from O ...edia|author1=Tanaka, Katsunori |author2=Fukase, Koichi|title=Lithium tetra(pentafluorophenyl)borate |encyclopedia=e-EROS Encyclopedia of Reagents for Organic Synthesis ...

...= Synthesis and Structure of the Dimethyl Sulfide Adducts of Mono- and Bis(pentafluorophenyl)borane | year = 2010 | last1 = Fuller | first1 = Anna-Marie | last2 = Hughe ...rapidly adds to the [[unsaturated bond]]s. The resulting [[organoborane]] compounds are useful [[Reaction intermediate|intermediates]] in [[organic synthesis]] ...

...cidity <ref>V. Gutmann, "Solvent effects on reactivities of organometallic compounds", ''Coord. Chem. Rev.'', 1976, '''18''', 225–255. [[doi: 10.1016/S0010-85 ...has been reviewed.<ref>I.B. Sivaev, V.L. Bregadze, "Lewis acidity of boron compounds", ''Coord. Chem. Rev.'', 2014, '''270/271''', 75-88. [[doi: 10.1016/j.ccr.2 ...

...hor6=Froehlich, R. |author7=Meyer, O. |title=Lewis Acid Properties of Tris(pentafluorophenyl)borane. Structure and Bonding in L-B(C₆F₅)<sub>3</sub ...rst2=Robert W. |date=1965-06-01 |title=The Ammonia and Alkylamine Addition Compounds of Carbon Monoxide Borane |url=http://dx.doi.org/10.1021/ja01089a009 |journ ...

'''Aluminylenes''' are a sub-class of [[aluminium(I) compounds]] that feature singly-coordinated [[aluminium]] atoms with a [[lone pair]] ...]] elements, but the lower stability and higher reactivity of aluminium(I) compounds makes for interesting chemistry.  The first aluminium(I) compound to be is ...

...nyl amido complexes, although the definition goes far beyond this class of compounds. The term CGC is frequently used in connection with other more or less rela ...y reaction with [[co-catalyst]]s, e.g. [[methylaluminoxane]] (MAO), [[tris(pentafluorophenyl)borane]]s, and [[trityl]] borates. The catalytic systems based on CGCs, how ...

Thus, a mixture of [[tricyclohexylphosphine]] (PCy₃) and [[tris(pentafluorophenyl)borane]] reacts with hydrogen to give the respective [[phosphonium]] and [[ ...that a mixture of [[tricyclohexylphosphine]] (PCy₃) and [[tris(pentafluorophenyl)borane]] reacts with H₂ to give the respective [[phosphonium]] a ...

...carbon-boron bond. The product of carboboration reactions are organoborane compounds which prove to be useful in [[organic synthesis]], containing both a new ca ...95 |title=l,l-Organoboration of alkynylsilicon, -germanium, -tin and -lead compounds |journal=Coordination Chemistry Reviews |volume=145 |page=125}}</ref> Howev ...

...[[halogen]] [[iodine]] forms a number of stable [[Organic compound|organic compounds]], in which iodine exhibits higher [[Formal charge|formal]] [[Oxidation sta These iodine compounds are [[hypervalency|hypervalent]] because the iodine atom formally contains ...

...2=Autrey |first2=Tom |date=2012-10-18 |title=Boron–nitrogen–hydrogen (BNH) compounds: recent developments in hydrogen storage, applications in hydrogenation and [[File:C-F activation by B=P 2.png|thumb|444x444px|C-F activation of [[tris(pentafluorophenyl)borane]] by [(tmp)(L)B=PMes*] (L = IMe₄)<ref name="Price-2017">{ ...

...=Evgeny |pages=1–33 |isbn=9780471238966 }}</ref> Many reactions of organic compounds with halogen involve autocatalytic radical [[reaction mechanism|mechanisms] ...s, Stuart Kauffman.</ref> Illustrative is the reaction amino adenosine and pentafluorophenyl ester in the presence of amino adenosine triacid ester (AATE). This experi ...

==Compounds== ...or3=Taylor, Mark S. |title=Borinic Acids: A Neglected Class of Organoboron Compounds for Recognition of Diols in Aqueous Solution|journal=Australian Journal of ...

...versus the other perhalobenzenes, resulting in lower aromaticity of those compounds compared to C₆F₆. ...irst3=R. |last4=Tatlow |first4=J. C. |date=1960 |title=Aromatic polyfluoro-compounds. Part VI. Penta- and 2,3,5,6-tetra-fluorothiophenol |journal=Journal of the ...

...rs.<ref>{{cite book |doi=10.1002/14356007.a19_545.pub2 |chapter=Phosphorus Compounds, Organic |title=Ullmann's Encyclopedia of Industrial Chemistry |year=2006 | ...ussRev>{{cite journal|title=Phosphine in the synthesis of organophosphorus compounds|first1=Boris A. |last1=Trofimov|first2=Svetlana N. |last2=Arbuzova|first3=N ...

...ore facile synthesis allowing a synthetic route to many low-valent gallium compounds. ...efits of Solid-State Analysis Aiding in the Synthesis of P→Ga Coordination Compounds|url=https://doi.org/10.1021/ic501139w|journal=Inorganic Chemistry|volume=53 ...

...um catalysts. A commonly used counter ion for borenium cations is tetrakis(pentafluorophenyl)borate, B(C₆F₅)₄⁻; however, o [[Category:Boron compounds]] ...

...tuent. FITC reacts with the [[amine]] groups of many biologically relevant compounds including intracellular proteins to form a thiourea linkage. *Others: [[carboxyfluorescein]], [[carboxyfluorescein succinimidyl ester]], [[Pentafluorophenyl esters]] (PFP), [[tetrafluorophenyl esters]] (TFP) are other useful reagent ...

...s such as using high pressures and low temperatures, or employing chemical compounds that release H₂ upon demand. While large amounts of hydrogen are ...atalyzed [[hydrogenation|dehydrogenation reactions]]. Illustrative storage compounds are hydrocarbons, [[boron hydride]]s, [[Hydrogen storage#Ammonia|ammonia]], ...

...ef>{{harvnb|Calvin|1969}}</ref>{{page needed|date=May 2022}} Some of these compounds like [[Hydrogen cyanide|hydrocyanic acid]] (HCN) have been proven in the ex ...sulfide and manganese sulfide in these ponds would have catalyzed organic compounds by abiotic photosynthesis.<ref>{{Cite journal |last1=Mulkidjanian |first1=A ...