Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Tarik J. Ozumerzifon"'
Autor:
Mei Ding, Mathieu Rouzières, Jeremy M. Smith, Martín Amoza, Joshua Telser, Wesley A. Hoffert, Tarik J. Ozumerzifon, David L. Tierney, Matthew P. Shores, Eliseo Ruiz, Anne K. Hickey, Maren Pink, Rodolphe Clérac
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2019, 25 (45), pp.10625-10632. ⟨10.1002/chem.201900799⟩
Universidad de Barcelona
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2019, 25 (45), pp.10625-10632. ⟨10.1002/chem.201900799⟩
International audience; The single-molecule magnet (SMM) properties of a series of ferrocenium complexes, [Fe(h5-C5R5)2]+ (R=Me, Bn), are reported. In the presence of an applied dc field, the slow dynamics of the magnetization in [Fe(h5-C5Me5)2]BArF
Autor:
Justin P. Joyce, Robert F. Higgins, Tarik J. Ozumerzifon, Jacek L. Kolanowski, Matthew P. Shores, Anthony K. Rappé
Publikováno v:
Inorganic Chemistry. 58:7785-7793
We present evidence of a spin-state change that accompanies desilylation reactions performed on two related Fe(II) iminopyridine coordination complexes. To probe these systems, we performed titrations with CsF in solution and analyzed the speciation
Autor:
Brooke N. Livesay, Christina M. Klug, Matthew P. Shores, Tarik J. Ozumerzifon, Anthony K. Rappé, Indrani Bhowmick
Publikováno v:
Dalton Transactions. 48:9117-9126
We report the syntheses and magnetic property characterizations of four mononuclear cobalt(ii) complex salts featuring a tripodal iminopyridine ligand with external anion receptor groups, [CoL5-ONHtBu]X2 (X = Cl (1), Br (2), I (3) and ClO4 (4)). Whil
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 156:323-327
Deamidation of asparagine (Asn) residues is one of the most common chemical degradation pathways observed in proteins. This reaction must be understood and controlled in therapeutic drug candidates, as chemical changes can affect their efficacy and s
Autor:
Robert F. Higgins, Justin P. Joyce, Tarik J. Ozumerzifon, Brooke N. Livesay, Matthew P. Shores, Anthony K. Rappé
Publikováno v:
Polyhedron. 143:193-200
We describe the syntheses, crystal structures and magnetic properties of several Co(II) complexes containing 4′-pyrrolidine-2,2′:6′,2″-terpyridine (pyrtpy) or 4′-triflouromethylsulfonate-2,2′:6′,2″-terpyridine (OTftpy) ligands: [(OTft
Autor:
Arnold L. Rheingold, Tarik J. Ozumerzifon, James McNeely, Linda H. Doerrer, Matthew P. Shores, Jesse L. Guillet, James A. Golen, Arunpatcha Nimthong-Roldán
Publikováno v:
Dalton Transactions. 46:5546-5557
Four new quasi-1D Ni2-lantern chain complexes of the form [Ni2(SOCR)4(L)]∞ (R = Ph, L = DABCO (1); R = Ph, L = pyz (2); R = CH3, L = DABCO (3); R = CH3, L = pyz (4)) were prepared from the reaction of [Ni2(SOCR)4(EtOH)], R = CH3 or Ph, with the N,N
Autor:
Indrani Bhowmick, Anthony K. Rappé, Tarik J. Ozumerzifon, William C. Spaller, Matthew P. Shores
Publikováno v:
Chemical Communications. 53:4211-4214
We present the syntheses and characterization of several salts of a trigonal prismatic cobalt(ii) complex with a 1,3,5-triaminocyclohexane (tach)-derived ditopic ligand. The air- and moisture-stable tetraphenylborate salt (2) shows slow magnetic rela
Publikováno v:
Organic Letters. 18:64-67
A variety of substituted indoles and benzofurans are accessed via a platinum catalyzed annulation and vinylogous addition of enol nucleophiles. Several β-dicarbonyl compounds participate in the reaction, as do α-nitro and α-cyano carbonyl species.
Publikováno v:
Organic letters. 19(1)
Formal syntheses of tetracyclic terpenoids frondosin B and liphagal are described. Both synthetic routes rely on the use of platinum-catalyzed α,β-unsaturated carbene formation for the key C–C bond forming transformations. The successful route to
Publikováno v:
ChemInform. 47
A variety of substituted indoles and benzofurans are accessed via a platinum catalyzed annulation and vinylogous addition of enol nucleophiles. Several β-dicarbonyl compounds participate in the reaction, as do α-nitro and α-cyano carbonyl species.