Mayr's Database Of Reactivity Parameters
AK Prof. Mayr

Diarylcarbenium Ions

For reactivities of structurally related compounds go to: Electrophiles » C-Electrophiles » Carbocations
Found 33 Molecules.
Molecule Solvent Reactivity Parameters Classification Reference (sort by title or year)
image of molecule

benzhydrylium ion Ph2CH+
0E Parameter: 5.47
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

(pcp)2CH+
0E Parameter: 5.48
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

pfp(Ph)CH+
0E Parameter: 5.20
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

(fur)2CH+
0E Parameter: -1.36
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

(ani)2CH+
0E Parameter: 0.00
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

(tol)2CH+
0E Parameter: 3.63
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

(pfa)2CH+
0E Parameter: -3.14
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

(mfa)2CH+
0E Parameter: -3.85
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

(dpa)2CH+
0E Parameter: -4.72
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

(mor)2CH+
0E Parameter: -5.53
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

(mpa)2CH+
0E Parameter: -5.89
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

(dma)2CH+
0E Parameter: -7.02
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

(pyr)2CH+
0E Parameter: -7.69
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

(thq)2CH+
0E Parameter: -8.22
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

(ind)2CH+
0E Parameter: -8.76
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

(jul)2CH+
0E Parameter: -9.45
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

(lil)2CH+
0E Parameter: -10.04
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

ani(pop)CH+
0E Parameter: 0.61
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

ani(Ph)CH+
0E Parameter: 2.11
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

ani(tol)CH+
0E Parameter: 1.48
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

pop(Ph)CH+
0E Parameter: 2.90
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

tol(Ph)CH+
0E Parameter: 4.43
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

(pfp)2CH+
0E Parameter: 5.01
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

(fur)(ani)CH+
0E Parameter: -0.81
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

(mfp)PhCH+
0E Parameter: 6.23
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

(tfm)PhCH+
0E Parameter: 6.70
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

(dfp)PhCH+
0E Parameter: 6.74
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

(mfp)2CH+
0E Parameter: 6.87
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

(dfp)(mfp)CH+
0E Parameter: 7.52
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

(tfm)2CH+
0E Parameter: 7.96
**J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

(dfp)2CH+
0E Parameter: 8.02
*J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

(Ftol)2CH+
0E Parameter: 5.24
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

pop(tol)CH+
0E Parameter: 2.16
***Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c