Search results for "KINETIC CONTROL"

Thermodynamic and kinetic control over the oxidation mechanism of the natural vanadyl porphyrin series (DPEP)VO in methylene chloride: electrogenerat…

2006

The electrochemical behavior of the natural (DPEP)VO series (where DPEP is the dianion deoxophylloerythroetioporphyrinate) is studied in methylene chloride. The investigated compounds, which were extracted from oil shales of Tarfaya (Morocco), exhibit a typical electrochemical behavior as compared to that of related synthetic vanadyl porphyrins. The electro-oxidation of (DPEP)VO is characterized by a splitting of the peaks when carried out at a glassy carbon electrode. This can be explained by two possible paths (CE and EC mechanisms) which are characterized by a “square diagram” where the chemical step, C, corresponds to a dimerization (radical–radical or substrate–substrate reaction). The…

ChemInform Abstract: First Reactions of Dialkoxycarbenium Tetrafluoroborates with Pyrroles, 5H-Dibenz(b,f)azepines, and Electron-Rich Arenes.

1990

Pyrrole (2a) and 2,5-dimethylpyrrole (2b) react with the dialkoxycarbenium tetrafluoroborates 1a-1c under kinetic control to yield the corresponding acylpyrrole derivatives. 5H-Dibenz[b,f]azepine (9a) and the 10,11-dihydro derivative 9b react only with the most electrophilic of the series of electrophiles tested, namely, diethoxycarbenium tetrafluoroborate (1a), to furnish the corresponding formyl derivatives. Similarly, in arene chemistry, the highly electron-rich N,N-dimethylaniline (13a) and 1,3,5-trimethoxybenzene (13b) are formylated by reaction with 1a.

Structural and metallo selectivity in the assembly of [2 × 2] grid-type metallosupramolecular species: Mechanisms and kinetic control

2011

An unsymmetrical bis(tridentate) ligand LH in which one binding site can be readily deprotonated forms a kinetically inert [Co(III)L(2)](+) complex which can be used as a "corner" species for the "Coupe du Roi" assembly of trans,trans-[Co(2)M(2)L(4)](6+) metallogrids (M = Fe(II), Co(II), Cu(II), Zn(II)). In the mixed Co(III)/Co(II) species, the oxidation states appear to be localised. In solution, the ligand LH forms octacationic, homometallic [2 × 2] grids with the individual labile metal ions Fe(II), Co(II), Cu(II), Zn(II), seemingly as mixtures of all possible isomers arising from the unsymmetrical nature of the ligand. In the solid state, however, [Zn(4)L(4)](CF(3)SO(3))(8)·4CH(3)CN cry…

Kinetically Controlled Stepwise Self-Assembly of AuI-Metallopeptides in Water

2018

The combination of attractive supramolecular interactions of a hydrophobic AuI-metallopeptide with the shielding effect of flexible oligoethylene glycol chains provides access to a stepwise self-assembly of a AuI-metalloamphiphile in water. Kinetic control of the supramolecular polymer morphology is achieved using a temperature-dependent assembly protocol, which yields low dispersity supramolecular polymers (metastable state I) or helical bundled nanorods (state II).

Strategies for Exploring Functions from Dynamic Combinatorial Libraries

2020

Ag2 and Ag3 clusters: synthesis, characterization, and interaction with DNA.

2015

Subnanometric samples, containing exclusively Ag2 and Ag3 clusters, were synthesized for the first time by kinetic control using an electrochemical technique without the use of surfactants or capping agents. By combination of thermodynamic and kinetic measurements and theoretical calculations, we show herein that Ag3 clusters interact with DNA through intercalation, inducing significant structural distortion to the DNA. The lifetime of Ag3 clusters in the intercalated position is two to three orders of magnitude longer than for classical organic intercalators, such as ethidium bromide or proflavine. Fil: Buceta, David. Universidad de Santiago de Compostela; España Fil: Busto, Natalia. Unive…

Untersuchungen zur Konfigurationsstabilität von Enolaten aus β‐Ketocarbonsäureestern

1988

Z- und E-Enole von β-Ketocarbonsaurederivaten 1a–c werden vollstandig und irreversibel deprotoniert, wobei unter Konfigurationserhalt (kinetische Kontrolle) die Enolate 2a–c entstehen. Abhangig von Gegenionen (Li, Na, K), Medium (THF, HMPT) und Temperatur kann anschliesend eine Z/E-Aquilibrierung eintreten. Auf dieser Basis last sich die Synthese von Enolethern und Enolestern auf die gewunschte Konfiguration hinsteuern. Investigations on the Stability of the Configuration of Enolates from β-ketocarboxylic Acid Esters Z- and E-enoles of β-ketocarboxylic acid esters 1a–c are completely and irreversibly deprotonated yielding the enolates 2a–c under retention of the configuration (kinetic contr…

Inside Back Cover: Kinetically Controlled Sequential Growth of Surface-Grafted Chiral Supramolecular Copolymers (Angew. Chem. Int. Ed. 25/2016)

2016

Strategies for Exploring Functions from Dynamic Combinatorial Libraries

2020

Dynamic combinatorial chemistry (DCC) is a powerful approach for creating complex chemical systems, giving access to the studies of complexity and exploration of functionality in synthetic systems. However, compared with more advanced living systems, the man‐made chemical systems are still less functional, due to their limited complexity and insufficient kinetic control. Here we start by introducing strategies to enrich the complexity of dynamic combinatorial libraries (DCLs) for exploiting unexpected functions by increasing the species of building blocks and/or templates used. Then, we discuss how dynamic isomerization of photo‐switchable molecules help DCLs increase and alter the systemic…