Literature DB >> 27885777

Variable Time Normalization Analysis: General Graphical Elucidation of Reaction Orders from Concentration Profiles.

Jordi Burés1.   

Abstract

The recent technological evolution of reaction monitoring techniques has not been paralleled by the development of modern kinetic analyses. The analyses currently used disregard part of the data acquired, thus requiring an increased number of experiments to obtain sufficient kinetic information for a given chemical reaction. Herein, we present a simple graphical analysis method that takes advantage of the data-rich results provided by modern reaction monitoring tools. This analysis uses a variable normalization of the time scale to enable the visual comparison of entire concentration reaction profiles. As a result, the order in each component of the reaction, as well as kobs  , is determined with just a few experiments using a simple and quick mathematical data treatment. This analysis facilitates the rapid extraction of relevant kinetic information and will be a valuable tool for the study of reaction mechanisms.
© 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  catalysis; kinetic analysis; reaction kinetics; reaction mechanisms; reaction order

Year:  2016        PMID: 27885777     DOI: 10.1002/anie.201609757

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  45 in total

1.  Oxidative nitrene transfer from azides to alkynes via Ti(ii)/Ti(iv) redox catalysis: formal [2+2+1] synthesis of pyrroles.

Authors:  Adam J Pearce; Xin Yi See; Ian A Tonks
Journal:  Chem Commun (Camb)       Date:  2018-06-19       Impact factor: 6.222

2.  Cobalt-Catalyzed Borylation of Fluorinated Arenes: Thermodynamic Control of C(sp2)-H Oxidative Addition Results in ortho-to-Fluorine Selectivity.

Authors:  Tyler P Pabst; Jennifer V Obligacion; Étienne Rochette; Iraklis Pappas; Paul J Chirik
Journal:  J Am Chem Soc       Date:  2019-09-16       Impact factor: 15.419

3.  Bis(imido)vanadium(V)-Catalyzed [2+2+1] Coupling of Alkynes and Azobenzenes Giving Multisubstituted Pyrroles.

Authors:  Kento Kawakita; Evan P Beaumier; Yuya Kakiuchi; Hayato Tsurugi; Ian A Tonks; Kazushi Mashima
Journal:  J Am Chem Soc       Date:  2019-02-11       Impact factor: 15.419

Review 4.  Catalytic, Enantioselective Sulfenofunctionalization of Alkenes: Development and Recent Advances.

Authors:  Anastassia Matviitsuk; Jesse L Panger; Scott E Denmark
Journal:  Angew Chem Int Ed Engl       Date:  2020-08-18       Impact factor: 15.336

5.  Unusual Kinetic Profiles for Lewis Base-Catalyzed Sulfenocyclization of ortho-Geranylphenols in Hexafluoroisopropyl Alcohol.

Authors:  Kevin A Robb; Soumitra V Athavale; Scott E Denmark
Journal:  Synlett       Date:  2019-08-07       Impact factor: 2.454

6.  Mechanism of Ti-Catalyzed Oxidative Nitrene Transfer in [2 + 2 + 1] Pyrrole Synthesis from Alkynes and Azobenzene.

Authors:  Zachary W Davis-Gilbert; Xuelan Wen; Jason D Goodpaster; Ian A Tonks
Journal:  J Am Chem Soc       Date:  2018-05-31       Impact factor: 15.419

7.  Cyclometalated Iridium-PhanePhos Complexes Are Active Catalysts in Enantioselective Allene-Fluoral Reductive Coupling and Related Alcohol-Mediated Carbonyl Additions That Form Acyclic Quaternary Carbon Stereocenters.

Authors:  Leyah A Schwartz; Michael Holmes; Gilmar A Brito; Théo P Gonçalves; Jeffery Richardson; J Craig Ruble; Kuo-Wei Huang; Michael J Krische
Journal:  J Am Chem Soc       Date:  2019-01-25       Impact factor: 15.419

8.  Aryl Amination Using Soluble Weak Base Enabled by a Water-Assisted Mechanism.

Authors:  Sii Hong Lau; Peng Yu; Liye Chen; Christina B Madsen-Duggan; Michael J Williams; Brad P Carrow
Journal:  J Am Chem Soc       Date:  2020-11-12       Impact factor: 15.419

9.  Mechanism of Ni-Catalyzed Reductive 1,2-Dicarbofunctionalization of Alkenes.

Authors:  Qiao Lin; Tianning Diao
Journal:  J Am Chem Soc       Date:  2019-10-28       Impact factor: 15.419

10.  Mechanistic Origins of Regioselectivity in Cobalt-Catalyzed C(sp2)-H Borylation of Benzoate Esters and Arylboronate Esters.

Authors:  Tyler P Pabst; Linda Quach; Kaitlyn T MacMillan; Paul J Chirik
Journal:  Chem       Date:  2020-12-09       Impact factor: 22.804

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