Coinage metals trinuclear metallocycles: old and new aspects of this class of compounds

Coinage metals trinuclear metallocycles: old and new aspects of this class of compounds Galassi R. a, Oumarou C. S. a, Omary A. M. b, Nesterov V. b, Burini A.a aSchool of Science and Technology, Chemistry Division, University of Camerino, Via S. Agostino 1, 62032 Camerino; e-mail: [email protected] b Department of Chemistry, University of North Texas, Denton, 1155 Union Circle, TX 76203, USA; e-mail: [email protected] Azoles such as imidazoles and pyrazoles are optimal bridging ligands to obtain C,N or N,N trinuclear coinage metals metallocycles. Since past decade till now, few worldwide research groups including us have focused their attention to their synthesis and characterization.[1] Moreover, the photophysical properties[2] the extended network of metallophilic bondings in the supramolecular structure and the pi-acid/pi-base chemistry[3] of these compounds directed the research to theoretical studies bringing to a better interpretation of the experimental behaviors.[4] Here we report the synthesis of new coinage metals metallocycles and their spectroscopic characterizations highlighting points of continuity with the previous analogs and new features for new perspective research lines. As in example, the 1-vinylimidazole resembles the acid-base chemistry of the 1-benzylimidazole gold(I) metallocycle, while substitution in position 4,5 of 1-benzylimidazole with electron-withdrawing group, do not allow the formation of metallocycles with the same synthethic route and mononuclear gold(I) derivatives have been obtained. The nature of the heterocycle and of the substituents, in addition to their position in the azolate ligand defines and tunes the properties of the final products. References: 1) Galassi, R.; Burini, A.; Omary-Rawanashed, M., Omary, M. A., Comm. Inorg. Chem. 2014, in submission. 2) Rawashdeh-Omary, M. A.; Omary, M. A.; Fackler Jr, J. P, Galassi R., Pietroni, B. R.; Burini, A. J. Am. Chem. Soc 2001, 123; 9689-9691. 3) Burini, A.;. Fackler Jr, J. P; Galassi R., Grant, T. A.. Omary, M. A; Rawashdeh-Omary, M. A.; Pietroni, B. R.; Staples R. J. J. Am. Chem. Soc., 2000; 11264-11265. 4) Galassi, R.; Ricci, S.; Burini, A.; Macchioni, A; Marmottini, F.; Tekarli, S. M.; Nesterov, N.V.; Omary, M. A. Inorg. Chem. 2013, 52, 14124-14137

Supramolecular Chemistry and photophysical Properties of a New Gold (I) Cyclic Trinuclear Complex, [Au(µ-C2,N3-1-vinylimidazole)]3

Supramolecular Chemistry and photophysical Properties of a New Gold (I) Cyclic Trinuclear Complex, [Au(µ-C2,N3-1-vinylimidazole)]3 R. Galassia, A. Burinia, C. S. Oumaroua, V. N. Nesterov b, M. A. Omary b. a Dipartimento di Scienze Chimica, Università di Camerino, Via Sant Agostino, 1, 62032 Camerino, Italia b Department of Chemistry, University of North Texas, Denton, TX 76203, USA email: [email protected] In the past years several cyclic trinuclear complexes (CTC’s) have been synthetized and characterized on the basis of the capacity of d10 transition metal ions to give bicoordinated linear compounds. This intriguing class of compounds display pi-acid/ pi-base properties that can be finely tuned by: the nature of the metal, the substituents on the ligand or the ligand itself. [1] These complexes are attractive building blocks to obtain supramolecular compounds showing interesting photopysical properties [2] or heterobimetallic cyclic trinuclear complexes with potential use in mixed-metal catalysis [3]. Here we report the synthesis of a novel gold (I) CTC, [Au(µ-C2,N3-1-vinylimidazole)]3, and the study of some photophysical properties of its supramolecular derivatives obtained by the intercalation of metal ions in between the metallocycles. [1] S.M. Terkali, T.R. Cundari, M.A. Omary, J. Am. Chem. Soc. 2008, 130, 1669 [2] a) A. Burini, R. Bravi, J. P. Fackler Jr, Galassi R., T. A. Grant, M. A. Omary, B. R. Pietroni, R. J. Staples . Inorg. Chem. 2000, 39; 3158.b) Burini A, Fackler J. P, JR, Galassi R., Grant T. A, Omary M. A, Rawashdeh-Omary M. A, Pietroni B. R, Staples R.J. J. Am. Chem. Soc. 2000, 122; 11264. [3] A. Mohamed, R. Galassi, F. Papa, A. Burini, J.P. Fackler , Jr. Inorg. Chem. 2006, 45, 7770-7776 [5] R. Galassi, S. Ricci, A. Burini, A. Macchioni, L. Rocchiagiani, F. Marmottini, S.M. Terkali, V.N. Nesterov, M.A. Omary, Inorg. Chem. 2013, 52, 14124-1413

Characterization of In Vivo Keratin 19 Phosphorylation on Tyrosine-391

Keratin polypeptide 19 (K19) is a type I intermediate filament protein that is expressed in stratified and simple-type epithelia. Although K19 is known to be phosphorylated on tyrosine residue(s), conclusive site-specific characterization of these residue(s) and identification potential kinases that may be involved has not been reported.In this study, biochemical, molecular and immunological approaches were undertaken in order to identify and characterize K19 tyrosine phosphorylation. Upon treatment with pervanadate, a tyrosine phosphatase inhibitor, human K19 (hK19) was phosphorylated on tyrosine 391, located in the 'tail' domain of the protein. K19 Y391 phosphorylation was confirmed using site-directed mutagenesis and cell transfection coupled with the generation of a K19 phospho (p)-Y391-specific rabbit antibody. The antibody also recognized mouse phospho-K19 (K19 pY394). This tyrosine residue is not phosphorylated under basal conditions, but becomes phosphorylated in the presence of Src kinase in vitro and in cells expressing constitutively-active Src. Pervanadate treatment in vivo resulted in phosphorylation of K19 Y394 and Y391 in colonic epithelial cells of non-transgenic mice and hK19-overexpressing mice, respectively.Human K19 tyrosine 391 is phosphorylated, potentially by Src kinase, and is the first well-defined tyrosine phosphorylation site of any keratin protein. The lack of detection of K19 pY391 in the absence of tyrosine phosphatase inhibition suggests that its phosphorylation is highly dynamic

Experimental visualization of breathing in fluorous metal–organic frameworks from single-crystal diffraction – functionalized MOFs for gas storage and separation

n/

4-(2-Methoxyphenyl)piperazin-1-ium 6-chloro-5-isopropyl-2,4-dioxopyrimidin-1-ide

In the cation of the title salt, C11H17N2O+.C7H8ClN2O2 -, the piperazine ring adopts a distorted chair conformation and contains a positively charged N atom with quaternary character. Its mean plane makes a dihedral angle of 42.36 (8)� with the phenyl ring of its 2-methoxyphenyl substituent. The 2,4-dioxopyrimidin-1-ide anion is generated by deprotonation of the N atom at the 1-position of the pyrimidinedione ring. Intramolecular C—H...O hydrogen bonds generate S(6) ring motifs in both the cation and the anion. In the crystal, N—H...O, N—H...N and C—H...O hydrogen bonds are also observed, resulting in a twodimensional network parallel to the ab plane. The crystal stability is further consolidated by weak C—H...n interactions

3-(Adamantan-1-yl)-4-benzyl-1H-1,2,4-triazole-5(4H)-thione

The title compound, C19H23N3S, is a functionalized triazoline-3-thione derivative. The benzyl ring is almost normal to the planar 1,2,4-triazole ring (r.m.s. deviation = 0.007 A°) with a dihedral angle of 86.90 (7)°. In the crystal, molecules are linked by pairs of N—H...S hydrogen bonds, forming inversion dimers that enclose R2/2(8) loops. The crystal packing is further stabilized by weak C—H...n interactions that link adjacent dimeric units into supramolecular chains extending along the a-axis direction

Crystal structure of 2-[(4-bromobenzyl)thio]-5-(5-bromothiophen-2-yl)-1,3,4-oxadiazole, C₁₃H₈Br₂N₂OS₂

C13H8Br2N2OS2, monoclinic, Pc (no. 7), a = 13.4050(4) angstrom, b = 4.7716(1) angstrom, c = 11.7303(4) angstrom, beta = 105.885( 3)degrees, V = 721.66(4) angstrom(3), Z = 2, R-gt(F) = 0.0294, wR(ref) (F-2 = 0.0808, T = 160K