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Sediment-water exchange of Mn, Fe, Ni and Zn in Galveston Bay, Texas

Marine chemistry, 2001-03, Vol.73 (3), p.215-231

2001

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Benthic Exchange of Nutrients in Galveston Bay, Texas

Estuaries, 2000-10, Vol.23 (5), p.647-661

2000

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Unimolecular Decompositions of Ionized Isopropyl Methyl Ether: An ab Initio and RRKM Study

Journal of the American Chemical Society, 1995-03, Vol.117 (9), p.2557-2564

1995

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Why ketonization is favored over enolization in 5-membered ring H-transfers by CH3C(OH+)CH2CH2 and in 6-membered ring H-transfers by CH3(COH+)CH2CH2CH2

International journal of mass spectrometry, 2006-03, Vol.249-250, p.120-129

2006

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Why CH3CH3+. formation competes with H. loss from ccco C3H6O+. isomers

Journal of the American Society for Mass Spectrometry, 2003-02, Vol.14 (2), p.136-142

2003

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Unimolecular Reactions of Ionized Alkanes: Theoretical Study of the Potential Energy Surface for CH3.bul. and CH4 Losses from Ionized Butane and Isobutane

Journal of the American Chemical Society, 1994-11, Vol.116 (24), p.11078-11088

1994

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Transition state ring sizes in H-transfers in closed shell aliphatic cations

International journal of mass spectrometry, 2007-10, Vol.266 (1), p.8-14

2007

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Ab initio calculation of structure and inversion in difluoramine and dimethylamine

Journal of the American Chemical Society, 1976-05, Vol.98 (11), p.3140-3143

1976

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Size effects in ion-neutral complex-mediated alkane eliminations from ionized aliphatic ethers

Journal of the American Society for Mass Spectrometry, 1991-08, Vol.2 (4), p.261-269

1991

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Trace metal analysis of natural waters by ICP-MS with on-line preconcentration and ultrasonic nebulization

Journal of analytical atomic spectrometry, 1999, Vol.14 (2), p.247-252

1999

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Why ketonization is favored over enolization in 5-membered ring H-transfers by CH 3C( OH +)CH 2C H 2 and in 6-membered ring H-transfers by CH 3(C OH +)CH 2CH 2C H 2

International journal of mass spectrometry, 2006, Vol.249, p.120-129

2006

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Why are smaller fragments preferentially lost from radical cations at low energies and larger ones at high energies?: An experimental and theoretical study

International journal of mass spectrometry, 2002-06, Vol.217 (1), p.23-44

2002

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CH4 Loss from (CH3)4N+ Revisited: How Does This High Energy Elimination Compete with •CH3 Loss?

European journal of mass spectrometry (Chichester, England), 2004-12, Vol.10 (6), p.767-773

2004

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CH 4 Loss from (CH 3 ) 4 N + Revisited: How Does This High Energy Elimination Compete with • CH 3 Loss?

European journal of mass spectrometry (Chichester, England), 2004-12, Vol.10 (6), p.767-773

2004

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Decompositions of ionized isopropyl methyl ether: complex-mediated and direct processes in unimolecular dissociations

Journal of physical chemistry (1952), 1988-03, Vol.92 (6), p.1524-1530

1988

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Why CH 3 CH 3 +· formation competes with h · loss from CCCO C 3 H 6 O +· isomers

Journal of the American Society for Mass Spectrometry, 2003-02, Vol.14 (2), p.136-142

2003

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Ion-neutral complexes as intermediates in the decompositions of C5H10O2.cntdot.+ isomers

Journal of the American Chemical Society, 1987-12, Vol.109 (25), p.7648-7653

1987

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Why CH 3CH 3+· formation competes with h · loss from CCCO C 3H 6O +· isomers

Journal of the American Society for Mass Spectrometry, 2003, Vol.14 (2), p.136-142

2003

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The effect of ion size on rate of dissociation: RRKM calculations on model large polypeptide ions

Journal of the American Society for Mass Spectrometry, 1993, Vol.4 (1), p.11-15

1993

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Why are smaller fragments preferentially lost from radical cations at low energies and larger ones at high energies?

International journal of mass spectrometry, 2002-06, Vol.217 (1-3), p.23-44

2002

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Nonergodic behavior, possibly due to an insufficient density of states, in the decompositions of .cntdot.CH2C(CO)OD

Journal of physical chemistry (1952), 1984-04, Vol.88 (8), p.1481-1485

1984

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Decompositions of the metastable [CH2C(OH)2]+.cntdot.ion. A test of the applicability of the energy randomization hypothesis to unimolecular fragmentations

Journal of physical chemistry (1952), 1979-05, Vol.83 (9), p.1142-1144

1979

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Preference for an ion-neutral complex-mediated pathway over a five-membered-ring H shift in the isomerization of CH 3 O + HCH 2 CH 2 · to CH 3 CH 2 CH 2 OH +· by Ab initio theory

Journal of the American Society for Mass Spectrometry, 1995-11, Vol.6 (11), p.1037-1046

1995

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Preference for an ion-neutral complex-mediated pathway over a five-membered-ring H shift in the isomerization of CH 3O +HCH 2CH 2 . to CH 3CH 2CH 2OH +. by Ab initio theory

Journal of the American Society for Mass Spectrometry, 1995, Vol.6 (11), p.1037-1046

1995

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Evaluation of AM1-calculated radical cation ion-neutral complexes

Journal of computational chemistry, 1993-12, Vol.14 (12), p.1561-1574

1993

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Sediment-water exchange of Mn, Fe, Ni and Zn in Galveston Bay, Texas

Benthic Exchange of Nutrients in Galveston Bay, Texas

Unimolecular Decompositions of Ionized Isopropyl Methyl Ether: An ab Initio and RRKM Study

Why ketonization is favored over enolization in 5-membered ring H-transfers by CH3C(OH+)CH2CH2 and in 6-membered ring H-transfers by CH3(COH+)CH2CH2CH2

Why CH3CH3+. formation competes with H. loss from ccco C3H6O+. isomers

Unimolecular Reactions of Ionized Alkanes: Theoretical Study of the Potential Energy Surface for CH3.bul. and CH4 Losses from Ionized Butane and Isobutane

Transition state ring sizes in H-transfers in closed shell aliphatic cations

Ab initio calculation of structure and inversion in difluoramine and dimethylamine

Size effects in ion-neutral complex-mediated alkane eliminations from ionized aliphatic ethers

Trace metal analysis of natural waters by ICP-MS with on-line preconcentration and ultrasonic nebulization

Why ketonization is favored over enolization in 5-membered ring H-transfers by CH 3C( OH +)CH 2C H 2 and in 6-membered ring H-transfers by CH 3(C OH +)CH 2CH 2C H 2

Why are smaller fragments preferentially lost from radical cations at low energies and larger ones at high energies?: An experimental and theoretical study

CH4 Loss from (CH3)4N+ Revisited: How Does This High Energy Elimination Compete with •CH3 Loss?

CH 4 Loss from (CH 3 ) 4 N + Revisited: How Does This High Energy Elimination Compete with • CH 3 Loss?

Decompositions of ionized isopropyl methyl ether: complex-mediated and direct processes in unimolecular dissociations

Why CH 3 CH 3 +· formation competes with h · loss from CCCO C 3 H 6 O +· isomers

Ion-neutral complexes as intermediates in the decompositions of C5H10O2.cntdot.+ isomers

Why CH 3CH 3+· formation competes with h · loss from CCCO C 3H 6O +· isomers

The effect of ion size on rate of dissociation: RRKM calculations on model large polypeptide ions

Why are smaller fragments preferentially lost from radical cations at low energies and larger ones at high energies?

Nonergodic behavior, possibly due to an insufficient density of states, in the decompositions of .cntdot.CH2C(CO)OD

Decompositions of the metastable [CH2C(OH)2]+.cntdot.ion. A test of the applicability of the energy randomization hypothesis to unimolecular fragmentations

Preference for an ion-neutral complex-mediated pathway over a five-membered-ring H shift in the isomerization of CH 3 O + HCH 2 CH 2 · to CH 3 CH 2 CH 2 OH +· by Ab initio theory

Preference for an ion-neutral complex-mediated pathway over a five-membered-ring H shift in the isomerization of CH 3O +HCH 2CH 2 . to CH 3CH 2CH 2OH +. by Ab initio theory

Evaluation of AM1-calculated radical cation ion-neutral complexes

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