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Synthesis and characterisation of a mesocyclic tripodal triamine ligand

Andrew D. Ure, Isabel Abánades Lázaro, Michelle Cottera and Aidan R. McDonald* The University of Dublin, Ireland Org. Biomol. Chem. 2015 , Advance Article DOI: 10.1039/C5OB01556A Meso- and macrocyclic polydentate amine ligands have been widely explored in oxidation catalysis and for the stabilization of unstable metal-superoxide, -peroxide, and -oxo intermediates. Herein we report on the design and synthesis of a novel mesocyclic, tripodal, triamine ligand that we believe will be an excellent addition to this field. We explored a number of synthetic procedures towards the mesocyclic asymmetric tetraalkylated ligand 1. We expect that 1 will bind metals in a facially capping manner, yielding complexes that display pseudo-tetrahedral geometry, potentially providing access to unprecedented late transition metal-oxo complexes (metal = Co, Ni, Cu). We describe the preparation of a library of mesocyclic polyamine synthons (8, 16, 17, 18, 19) that are precursors in the synthesis of 1. ...

Synthesis and characterization of M(II) (M = Mn, Fe and Co) azafulvene complexes and their X3− derivatives

分子内水素結合をする事のできるトライポッド配位子の報告です。 コンセプチュアルには、増田先生のtpaにピバルアミドを三つ付けたもの( Inorganica Chimica Acta  324 (2001) 108 )、それにつづくボロヴィックのbueaの流れで、そこまで目新しいところは無いと思います 。 NHの酸性度が十分に高いとすれば、N–になった時の共役系の変化が見れて面白いのかもしれません。 Ellen M. Matson , a      Yun Ji Park , a      Jeffery A. Bertke a  and   Alison R. Fout * a    School of Chemical Sciences, University of Illinois at Urbana-Champaign, 600 S. Mathews Ave., Urbana, Illinois 61801, USA. E-mail:  fout@illinois.edu Dalton Trans. , 2015, 44 , 10377-10384 DOI:  10.1039/C5DT00985E Received 11 Mar 2015, Accepted 05 May 2015 First published online 13 May 2015 PDF     Rich HTML The syntheses of M( II ) (M = Mn, Fe, Co) complexes bearing the tris(5-cycloaminoazafulvene-2-methyl)amine (H 3 N(afa Cy ) 3 ) ligand in its datively coordinated, tautomeric form is reported. The metal–azafulvene complexes [N(afa Cy ) 3 M](OTf) 2  are generated in high yields, fea...

Redox-induced fluoride ligand dissociation stabilized by intramolecular hydrogen bonding

RSC - Chem. Commun. latest articles  by Cameron M. Moore  /   21d   //   keep unread   //   hide   //   preview Chem. Commun. , 2014, Advance Article DOI : 10.1039/C4CC06832G, Communication Cameron M. Moore, Nathaniel K. Szymczak Appended hydrogen-bonding groups enable the reduction and F -  capture of a tripodal copper fluoride complex. To cite this article before page numbers are assigned, use the DOI form of citation above. The content of this RSS Feed (c) The Royal Society of Chemistry http://pubs.rsc.org/en/Content/ArticleLanding/2014/CC/C4CC06832G#!divAbstract

Probing the role of an FeIV tetrazene in catalytic aziridination

配位子が結構かっこいい S. Alan Cramer , a      Raúl Hernández Sánchez , b    Desirae F. Brakhage a  and     David M. Jenkins * a    Show Affiliations Chem. Commun. , 2014, 50 , 13967-13970 DOI:  10.1039/C4CC05124F Received 03 Jul 2014, Accepted 09 Sep 2014 First published online 30 Sep 2014 Share on citu Sh re PDF Rich HTML An iron( IV ) tetrazene complex has been synthesized that is an important addition to a previously proposed catalytic aziridination cycle. It provides two key insights about the aziridination: an iron( IV ) imide is formed and this imide can bind an additional ligand in the  cis  position.

A Versatile Tripodal Cu(I) Reagent for C–N Bond Construction via Nitrene-Transfer Chemistry: Catalytic Perspectives and Mechanistic Insights on C–H Aminations/Amidinations and Olefin Aziridinations

Journal of the American Chemical Society: Latest Articles (ACS Publications)  by Vivek Bagchi, Patrina Paraskevopoulou, Purak Das, Lingyu Chi, Qiuwen Wang, Amitava Choudhury, Jennifer S. Mathieson, Leroy Cronin, Daniel B. Pardue, Thomas R. Cundari, George Mitrikas, Yiannis Sanakis and Pericles Stavropoulos  /   4h   //   keep unread   //   hide   //   preview Journal of the American Chemical Society DOI: 10.1021/ja503869j Visit Website

Synthesis of a “Super Bulky” Guanidinate Possessing an Expandable Coordination Pocket

Inorganic Chemistry: Latest Articles (ACS Publications)  by Arnab K. Maity, Skye Fortier, Leonel Griego and Alejandro J. Metta-Magaña  /   18d   //   keep unread   //   hide   //   preview Inorganic Chemistry DOI: 10.1021/ic501219q Visit Website

Uranium(IV) Halide (F−, Cl−, Br−, and I−) Monoarene Complexes

Inorganic Chemistry: Latest Articles (ACS Publications)  by Dominik P. Halter, Henry S. La Pierre, Frank W. Heinemann and Karsten Meyer  /   2d   //   keep unread   //   hide   //   preview Inorganic Chemistry DOI: 10.1021/ic501011p Visit Website

Atom Transfer Radical Polymerization (ATRP) and Organometallic Mediated Radical Polymerization (OMRP) of Styrene Mediated by Diaminobis(phenolato)iron(II) Complexes: A DFT Study

Inorganic Chemistry: Latest Articles (ACS Publications)  by Rinaldo Poli and Michael P. Shaver  /   1d   //   keep unread   //   hide   //   preview Inorganic Chemistry DOI: 10.1021/ic5009347 Synopsis The action of a diaminobis(phenolato) iron system as a controlling agent for the polymerization of styrene has been addressed by a DFT study, supporting the view that the system operates by combined ATRP and OMRP moderating equilibria. The study also addresses the electronic effect of ligand substituents on the controlling ability, the effect of pressure on rates through volume calculations, and the effect of the spin state change on the activation barriers for the trapping processes. View:  ACS ActiveView PDF  |  PDF  |  PDF w/ Links  |  Full Text HTML

Hydrogen Evolution Catalyzed by an Iron Polypyridyl Complex in Aqueous Solutions

Communication Previous Article Next Article Table of Contents ACS ActiveView PDF Hi-Res Print, Annotate, Reference QuickView PDF  [833 KB] PDF w/ Links [216 KB] Full Text HTML Abstract Supporting Info -> Figures Reference QuickView Add to ACS ChemWorx G. P. Connor   † ,  K. J. Mayer   † ,  C. S. Tribble   † , and  W. R. McNamara   * † †  Department of Chemistry,  College of William and Mary , PO Box 8795, Williamsburg, Virginia 23187-8795,  United States Inorg. Chem. ,  2014 ,  53  (11), pp 5408–5410 DOI:  10.1021/ic500069c Publication Date (Web): May 21, 2014 Copyright © 2014 American Chemical Society *E-mail:  wrmcnamara@wm.edu . Synopsis An iron complex containing a tetradentate monophenolate ligand has been found to be highly active for the electrocatalytic reduction of protons to hydrogen gas. The catalytic activity is enhanced in the prese...

Significant Influence of Coligands Toward Varying Coordination Modes of 2,2′-Bipyridine-3,3′-diol in Ruthenium Complexes

ACS ActiveView PDF Hi-Res Print, Annotate, Reference QuickView PDF  [2571 KB] PDF w/ Links [601 KB] Full Text HTML Abstract Supporting Info -> Figures Reference QuickView Add to ACS ChemWorx Prabir Ghosh   † ,  Prasenjit Mondal   † ,  Ritwika Ray   † , Ankita Das   † ,  Sukdev Bag   † ,  Shaikh M. Mobin   ‡ , and  Goutam Kumar Lahiri   * † †  Department of Chemistry,  Indian Institute of Technology Bombay , Powai, Mumbai 400076,  India ‡  Discipline of Chemistry, School of Basic Sciences, Indian Institute of Technology Indore , Indore 452017, India Inorg. Chem. , Article ASAP DOI:  10.1021/ic5004676 Publication Date (Web): May 22, 2014 Copyright © 2014 American Chemical Society *E-mail:  lahiri@chem.iitb.ac.in . Phone:  +91 22 25767159 . Fax:  +91 22 25723480 . Synopsis The strongly π-accepting phenylazopyridine in 2 facilitates the s...

Isolation of Iron(II) Aqua and Hydroxyl Complexes Featuring a Tripodal H-bond Donor and Acceptor Ligand

Ellen M. Matson   ,  Jeffrey A. Bertke   , and  Alison R. Fout   * School of Chemical Sciences,  University of Illinois at Urbana−Champaign , 600 S. Mathews Avenue Urbana, Illinois 61801,  United States Inorg. Chem. , Article ASAP DOI:  10.1021/ic500102c Publication Date (Web): April 23, 2014 Copyright © 2014 American Chemical Society *E-mail:  fout@illinois.edu . Synopsis A tripodal ligand platform, tris(5-cycloiminopyrrol-2-ylmethyl)amine (H3[N(piCy)3]) is reported. The ability of the ligand to tautomerize to the amino azafulvene H3[N(afaCy)3] upon substrate addition is evident in the isolation of a series of iron(II) complexes. The combined data for the iron complexes establishes that each arm of the tripodal ligand can tautomerize independently, depending on electronic needs of the iron center and substrate coordination. Abstract A tripodal ligand platform, tris(5-cycloiminopyrrol-2-ylmethyl)amine (H 3 [N(pi...

Iron(II) complexes of 2,6-di(1H-pyrazol-3-yl)-pyridine derivatives with hydrogen bonding and sterically bulky substituents

Thomas D. Roberts , a      Marc A. Little , a    Laurence J. Kershaw Cook a  and     Malcolm A. Halcrow * a    Show Affiliations Dalton Trans. , 2014, Advance Article DOI:  10.1039/C4DT00355A Received 03 Feb 2014, Accepted 30 Mar 2014 First published online 31 Mar 2014 | | Share on citeulike | Share on facebook | Share on twitter | | More PDF Rich HTML    Send PDF to Kindle Download Citation BibTex   EndNote   MEDLINE   ProCite   ReferenceManager   RefWorks   RIS   Request Permissions Abstract Cited by Related Content Metrics Syntheses of 2,6-di(5-aminopyrazol-3-yl)pyridine (L 1 ), 2,6-di(5- tert butylcarboxamidopyrazol-3-yl)pyridine (L 2 ), 2,6-di(5- tert butylpyrazol-3-yl)pyridine (L 3 ), 2-(5- tert butylpyrazol-3-yl)-6-(5-methylpyrazol-3-yl)pyridine (L 4 ) and 2-(5- tert butylpyrazol-3-yl)-6-(5-amin...