Phosphorus and Olefin Substituent Effects on the Insertion Chemistry of Nickel(II) Hydride Complexes Containing Amido Diphosphine Ligands

2008 ◽  
Vol 27 (13) ◽  
pp. 3082-3093 ◽  
Author(s):  
Lan-Chang Liang ◽  
Pin-Shu Chien ◽  
Pei-Ying Lee
Keyword(s):  
Substituent Effects ◽  
Diphosphine Ligands ◽  
Hydride Complexes

Electrochemical oxidation of H2 catalyzed by ruthenium hydride complexes bearing P2N2 ligands with pendant amines as proton relays

2014 ◽  
Vol 7 (11) ◽  
pp. 3630-3639 ◽  
Author(s):  
Tianbiao Liu ◽  
Mary Rakowski DuBois ◽  
Daniel L. DuBois ◽  
R. Morris Bullock
Keyword(s):  
Electrochemical Oxidation ◽  
Chemical Bond ◽  
Bond Energy ◽  
Diphosphine Ligands ◽  
Ruthenium Hydride ◽  
Hydride Complexes ◽  
New Class ◽  
Oxidation Of H2

A new class of Ru electrocatalysts containing P2N2 diphosphine ligands with pendant amines converts the chemical bond energy of H2 to electricity.

Substituent Effects on Reductive Elimination from Disubstituted Aryl Hydride Complexes: Mechanistic and Thermodynamic Considerations

1995 ◽  
Vol 14 (12) ◽  
pp. 5677-5685 ◽  
Author(s):  
Anthony D. Selmeczy ◽  
William D. Jones ◽  
Robert Osman ◽  
Robin Perutz
Keyword(s):  
Substituent Effects ◽  
Reductive Elimination ◽  
Hydride Complexes

Substituent effects and solvents

1992 ◽  
Vol 89 ◽  
pp. 1567-1571
Author(s):  
O Pytela ◽  
M Ludwig
Keyword(s):  
Substituent Effects

Substituent Effects on the Thermal Decomposition of Phosphate Esters on Ferrous Surfaces

2019 ◽  
Author(s):  
James Ewen ◽  
Carlos Ayestaran Latorre ◽  
Arash Khajeh ◽  
Joshua Moore ◽  
Joseph Remias ◽  
...  
Keyword(s):  
Thermal Decomposition ◽  
Film Formation ◽  
Substituent Effects ◽  
Vapour Phase ◽  
Industrial Applications ◽  
Phosphate Esters ◽  
Antiwear Additives ◽  
Formation Mechanisms ◽  
Phosphate Ester ◽  
Wide Range

<p>Phosphate esters have a wide range of industrial applications, for example in tribology where they are used as vapour phase lubricants and antiwear additives. To rationally design phosphate esters with improved tribological performance, an atomic-level understanding of their film formation mechanisms is required. One important aspect is the thermal decomposition of phosphate esters on steel surfaces, since this initiates film formation. In this study, ReaxFF molecular dynamics simulations are used to study the thermal decomposition of phosphate esters with different substituents on several ferrous surfaces. On Fe<sub>3</sub>O<sub>4</sub>(001) and α-Fe(110), chemisorption interactions between the phosphate esters and the surfaces occur even at room temperature, and the number of molecule-surface bonds increases as the temperature is increased from 300 to 1000 K. Conversely, on hydroxylated, amorphous Fe<sub>3</sub>O<sub>4</sub>, most of the molecules are physisorbed, even at high temperature. Thermal decomposition rates were much higher on Fe<sub>3</sub>O<sub>4</sub>(001) and particularly α-Fe(110) compared to hydroxylated, amorphous Fe<sub>3</sub>O<sub>4</sub>. This suggests that water passivates ferrous surfaces and inhibits phosphate ester chemisorption, decomposition, and ultimately film formation. On Fe<sub>3</sub>O<sub>4</sub>(001), thermal decomposition proceeds mainly through C-O cleavage (to form surface alkyl and aryl groups) and C-H cleavage (to form surface hydroxyls). The onset temperature for C-O cleavage on Fe<sub>3</sub>O<sub>4</sub>(001) increases in the order: tertiary alkyl < secondary alkyl < primary linear alkyl ≈ primary branched alkyl < aryl. This order is in agreement with experimental observations for the thermal stability of antiwear additives with similar substituents. The results highlight surface and substituent effects on the thermal decomposition of phosphate esters which should be helpful for the design of new molecules with improved performance.</p>

Chemistry of Unsymmetrical C1-Substituted Oxabenzonorbornadienes

2021 ◽  
Vol 17 ◽  
Author(s):  
Austin Pounder ◽  
Angel Ho ◽  
Matthew Macleod ◽  
William Tam
Keyword(s):  
Transition Metal ◽  
Metal Complexes ◽  
Transition Metal Complexes ◽  
Substituent Effects ◽  
Face Selectivity ◽  
Transition Metal Catalyzed ◽  
Catalyzed Reactions ◽  
Metal Catalyzed ◽  
Synthetic Intermediate

: Oxabenzonorbornadiene (OBD) is a useful synthetic intermediate which can be readily activated by transition metal complexes with great face selectivity due to its dual-faced nature and intrinsic angle strain on the alkene. To date, the understanding of transition-metal catalyzed reactions of OBD itself has burgeoned; however, this has not been the case for unsymmetrical OBDs. Throughout the development of these reactions, the nature of C1-substituent has proven to have a profound effect on both the reactivity and selectivity of the outcome of the reaction. Upon substitution, different modes of reactivity arise, contributing to the possibility of multiple stereo-, regio-, and in extreme cases, constitutional isomers which can provide unique means of constructing a variety of synthetically useful cyclic frameworks. To maximize selectivity, an understanding of bridgehead substituent effects is crucial. To that end, this review outlines hitherto reported examples of bridgehead substituent effects on the chemistry of unsymmetrical C1-substituted OBDs.

Influence of solvents on transmission of substituent effects by the oxygen and sulfur bridges

1974 ◽  
Vol 39 (7) ◽  
pp. 1862-1868 ◽  
Author(s):  
A. Perjéssy ◽  
G. Melikian ◽  
P. Hrnčiar ◽  
M. Lácová
Keyword(s):  
Substituent Effects ◽  
Influence Of Solvents

Substituent effects in 1,3-indanediones

1982 ◽  
Vol 47 (5) ◽  
pp. 1486-1493 ◽  
Author(s):  
Alexander Perjéssy
Keyword(s):  
Substituent Effects ◽  
Empirical Equations ◽  
Substituent Constants ◽  
Complex Structural

The carbonyl stretching frequencies correlate well with substituent constants in a series of 166 1,3-indanediones using improved and extended Seth-Paul-Van Duyse equation. Transmissive factors and group electronegativities have been used to find empirical equations for calculation of substituent constants of more complex structural fragments.

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