Determination of pKR+ values for cyclobutadieneiron tricarbonyl-substituted carbocations
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Reference19 articles.
1. The cyclobutadienyl-iron tricarbonyl carbinyl cation
2. Structure of .alpha.-cyclobutadienyliron tricarbonyl carbonium ions
3. A 13C nuclear magnetic resonance study of cyclobutadieneirontricarbonyl-substituted carbonium ions
4. Carbonium Ions. I. An Acidity Function (C0) Derived from Arylcarbonium Ion Equilibria1
5. Aqueous trifluoroacetic acid as a medium for organic reactions. I. Acidity functions and the identity of the manganese(VII) species found in powerfully acidic media
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1. Iron: Organometallic ChemistryBased in part on the article Iron: Organometallic Chemistry by James R. Green which appeared in theEncyclopedia of Inorganic Chemistry, First Edition.;Encyclopedia of Inorganic and Bioinorganic Chemistry;2011-12-15
2. Iron: Organometallic ChemistryBased in part on the article Iron: Organometallic Chemistry by James R. Green which appeared in theEncyclopedia of Inorganic Chemistry, First Edition.;Encyclopedia of Inorganic Chemistry;2006-03-15
3. Schwächung der Aromatizität des 5-Dibenzo[a,d]cycloheptenylium-Ions durch Komplexierung mit (CO)3Cr;Angewandte Chemie;2006-01-17
4. The pK(R+) values for coordinated propargyl cations [Cp2M2(CO)(4)(mu-eta(2),eta(3)-HC equivalent to(CCRR2)-R-1)](+) (M = Mo, W);Russian Chemical Bulletin;2003
5. Tricarbonyl(cyclobutadiene)iron;Encyclopedia of Reagents for Organic Synthesis;2001-04-15
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