Electro-inductive effect: Electrodes as functional groups with tunable electronic properties
暂无分享,去创建一个
M. Baik | S. Han | Hyun Kyong Shon | T. Lee | J. G. Son | Joon Heo | H. Ahn | Joonghee Won
[1] M. Baik,et al. Data for the paper: "Electro-inductive effect: electrodes as functional groups with tunable electronic properties" , 2020 .
[2] S. Bell,et al. Towards Reliable and Quantitative Surface‐Enhanced Raman Scattering (SERS): From Key Parameters to Good Analytical Practice , 2020, Angewandte Chemie.
[3] Haixia Li,et al. Is the Suzuki-Miyaura Cross-Coupling Reaction in the Presence of Pd Nanoparticles Heterogeneously or Homogeneously Catalyzed? An Interfacial Surface-Enhanced Raman Spectroscopy Study. , 2019, The journal of physical chemistry letters.
[4] J. Dawlaty,et al. Electrodes as Polarizing Functional Groups: Correlation between Hammett Parameters and Electrochemical Polarization , 2019, The Journal of Physical Chemistry C.
[5] A. Haes,et al. Importance of Tilt Angles of Adsorbed Aromatic Molecules on Nanoparticle Rattle SERS Substrates , 2016 .
[6] S. Boxer,et al. Extreme electric fields power catalysis in the active site of ketosteroid isomerase , 2014, Science.
[7] F. Palazón,et al. Carbodiimide/NHS derivatization of COOH-terminated SAMs: activation or byproduct formation? , 2014, Langmuir : the ACS journal of surfaces and colloids.
[8] Jing Zhang,et al. Jaguar: A high-performance quantum chemistry software program with strengths in life and materials sciences , 2013 .
[9] C. Amatore,et al. The triple role of fluoride ions in palladium-catalyzed Suzuki-Miyaura reactions: unprecedented transmetalation from [ArPdFL2] complexes. , 2012, Angewandte Chemie.
[10] C. Amatore,et al. Kinetic data for the transmetalation/reductive elimination in palladium-catalyzed Suzuki-Miyaura reactions: unexpected triple role of hydroxide ions used as base. , 2011, Chemistry.
[11] R. Salvarezza,et al. Self-assembled monolayers of thiols and dithiols on gold: new challenges for a well-known system. , 2010, Chemical Society reviews.
[12] P. Allongue,et al. Semiquantitative study of the EDC/NHS activation of acid terminal groups at modified porous silicon surfaces. , 2010, Langmuir : the ACS journal of surfaces and colloids.
[13] M. Bradley,et al. Amide bond formation: beyond the myth of coupling reagents. , 2009, Chemical Society reviews.
[14] M. Mitchell,et al. Reaction Progress Analysis: Powerful Tool for Understanding Suzuki―Miyaura Reaction and Control of Polychlorobiphenyl Impurity , 2009 .
[15] S. Buchwald,et al. Water-mediated catalyst preactivation: an efficient protocol for C-N cross-coupling reactions. , 2008, Organic letters.
[16] J. Hartwig. Electronic effects on reductive elimination to form carbon-carbon and carbon-heteroatom bonds from palladium(II) complexes. , 2007, Inorganic chemistry.
[17] T. Willey,et al. Effect of ring substitution position on the structural conformation of mercaptobenzoic acid self-assembled monolayers on Au(111). , 2006, Langmuir : the ACS journal of surfaces and colloids.
[18] T. Ohsaka,et al. Multiple voltammetric waves for reductive desorption of cysteine and 4-mercaptobenzoic acid monolayers self-assembled on gold substrates , 2003 .
[19] J. Lahann,et al. A Reversibly Switching Surface , 2003, Science.
[20] M. Pelletier,et al. Quantitative Analysis Using Raman Spectrometry , 2003, Applied spectroscopy.
[21] De‐Yin Wu,et al. Surface-Enhanced Raman Scattering: From Noble to Transition Metals and from Rough Surfaces to Ordered Nanostructures , 2002 .
[22] M. Porter,et al. Effects of Packing and Orientation on the Hydrolysis of Ester Monolayers on Gold , 2001 .
[23] Buchwald,et al. A Highly Active Catalyst for the Room-Temperature Amination and Suzuki Coupling of Aryl Chlorides. , 1999, Angewandte Chemie.
[24] Seokmin Shin,et al. Molecular Dynamics Simulation of Benzenethiolate and Benzyl Mercaptide on Au(111) , 1999 .
[25] A. Campion,et al. Surface-enhanced Raman scattering , 1998 .
[26] A. Brolo,et al. Relationship between SERS intensity and both surface coverage and morphology for pyrazine adsorbed on a polycrystalline gold electrode , 1998 .
[27] G. Whitesides,et al. Formation and Reaction of Interchain Carboxylic Anhydride Groups on Self-Assembled Monolayers on Gold , 1997 .
[28] T. Schneider,et al. Electrochemical quartz crystal microbalance studies of adsorption and desorption of self-assembled monolayers of alkyl thiols on gold , 1993 .
[29] A. Becke. Density-functional thermochemistry. III. The role of exact exchange , 1993 .
[30] F. Ozawa,et al. Generation of Tertiary Phosphine-Coordinated Pd(0) Species from Pd(OAc)2 in the Catalytic Heck Reaction , 1992 .
[31] Parr,et al. Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density. , 1988, Physical review. B, Condensed matter.
[32] Norio Miyaura,et al. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides , 1980 .
[33] J. Pople,et al. Self‐Consistent Molecular‐Orbital Methods. IX. An Extended Gaussian‐Type Basis for Molecular‐Orbital Studies of Organic Molecules , 1971 .
[34] S. Boxer,et al. Stark realities. , 2009, The journal of physical chemistry. B.
[35] J. Bukowska,et al. Surface‐enhanced Raman scattering (SERS) of 4‐mercaptobenzoic acid on silver and gold substrates , 2003 .
[36] G. Socrates,et al. Infrared and Raman characteristic group frequencies : tables and charts , 2001 .
[37] Ralph G. Nuzzo,et al. Fundamental studies of microscopic wetting on organic surfaces. 1. Formation and structural characterization of a self-consistent series of polyfunctional organic monolayers , 1990 .
[38] R. Parr. Density-functional theory of atoms and molecules , 1989 .
[39] G. Varsányi,et al. Vibrational spectra of benzene derivatives , 1969 .
[40] G. Varsányi. 3 – NORMAL VIBRATIONS OF BENZENE AND ITS DERIVATIVES , 1969 .
[41] L. Hammett. The Effect of Structure upon the Reactions of Organic Compounds. Benzene Derivatives , 1937 .