Literature DB >> 21384822

Alternative demetalation method for Cu(I)-phenanthroline-based catenanes and rotaxanes.

Jackson D Megiatto1, David I Schuster.   

Abstract

A new and less hazardous procedure for demetalation of Cu(I)-phenanthroline-based interlocked molecules, using aqueous NH(4)OH rather than toxic KCN, has been developed. The conditions are compatible with materials containing nucleophile-sensitive appended groups such as C(60), and coordinating moieties such as zinc(II)-porphyrins.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21384822      PMCID: PMC3070403          DOI: 10.1021/ol200304d

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  11 in total

1.  Convergent synthesis and photophysics of [60]fullerene/porphyrin-based rotaxanes.

Authors:  Ke Li; David I Schuster; Dirk M Guldi; M Angeles Herranz; Luis Echegoyen
Journal:  J Am Chem Soc       Date:  2004-03-24       Impact factor: 15.419

2.  [2]Catenanes decorated with porphyrin and [60]fullerene groups: design, convergent synthesis, and photoinduced processes.

Authors:  Jackson D Megiatto; David I Schuster; Silke Abwandner; Gustavo de Miguel; Dirk M Guldi
Journal:  J Am Chem Soc       Date:  2010-03-24       Impact factor: 15.419

3.  Synthesis of Catenane Structures via Ring-Closing Metathesis.

Authors:  Marcus Weck; Bernhard Mohr; Jean-Pierre Sauvage; Robert H. Grubbs
Journal:  J Org Chem       Date:  1999-07-23       Impact factor: 4.354

4.  Convergent synthesis and photoinduced processes in multi-chromophoric rotaxanes.

Authors:  Jackson D Megiatto; Ke Li; David I Schuster; Amit Palkar; M Ángeles Herranz; Luis Echegoyen; Silke Abwandner; Gustavo de Miguel; Dirk M Guldi
Journal:  J Phys Chem B       Date:  2010-06-02       Impact factor: 2.991

5.  General method for synthesis of functionalized macrocycles and catenanes utilizing "click" chemistry.

Authors:  Jackson D Megiatto; David I Schuster
Journal:  J Am Chem Soc       Date:  2008-09-04       Impact factor: 15.419

6.  Polypseudorotaxanes via ring-opening metathesis polymerizations of [2]catenanes.

Authors:  Songsu Kang; Brandon M Berkshire; Zheng Xue; Manav Gupta; Christianah Layode; Preston A May; Michael F Mayer
Journal:  J Am Chem Soc       Date:  2008-10-22       Impact factor: 15.419

7.  Bilability is defined when one electron is used to switch between concerted and stepwise pathways in Cu(I)-based bistable [2/3]pseudorotaxanes.

Authors:  Andrew I Share; Kumar Parimal; Amar H Flood
Journal:  J Am Chem Soc       Date:  2010-02-10       Impact factor: 15.419

8.  Efficient one-pot synthesis of rotaxanes bearing electron donors and [60]fullerene.

Authors:  Jackson D Megiatto; Robert Spencer; David I Schuster
Journal:  Org Lett       Date:  2009-09-17       Impact factor: 6.005

9.  "Click" methodology for synthesis of functionalized [3]catenanes: toward higher interlocked structures.

Authors:  Jackson D Megiatto; David I Schuster
Journal:  Chemistry       Date:  2009       Impact factor: 5.236

10.  Design and synthesis of porphyrin-containing catenanes and rotaxanes.

Authors:  Jonathan A Faiz; Valérie Heitz; Jean-Pierre Sauvage
Journal:  Chem Soc Rev       Date:  2008-11-24       Impact factor: 54.564

View more
  3 in total

1.  Topological and Conformational Effects on Electron Transfer Dynamics in Porphyrin-[60]Fullerene Interlocked Systems.

Authors:  Jackson D Megiatto; David I Schuster; Gustavo de Miguel; Silke Wolfrum; Dirk M Guldi
Journal:  Chem Mater       Date:  2012-06-18       Impact factor: 9.811

2.  Multistep energy and electron transfer processes in novel rotaxane donor-acceptor hybrids generating microsecond-lived charge separated states.

Authors:  Sabrina V Kirner; Christian Henkel; Dirk M Guldi; Jackson D Megiatto; David I Schuster
Journal:  Chem Sci       Date:  2015-10-02       Impact factor: 9.825

3.  Porphyrin-Polyyne [3]- and [5]Rotaxanes.

Authors:  Daniel R Kohn; Levon D Movsisyan; Amber L Thompson; Harry L Anderson
Journal:  Org Lett       Date:  2017-01-05       Impact factor: 6.005

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.