Manuel de littérature classique ancienne : contenant: I. L'archéologie ; II. Une notice des auteurs classiques ; III. La mythologie ; IV. V. Les antiquités grecques et romaines /

Contiene: T. I -- T. II.

Josephi Weissenbach ... De Eloquentia Patrum libri XIII : in usum ecclesiasticorum : volumen IV, operis libros IV & V complectens.

Mode of access: Internet.

An essay on the interpretation of Romans, Chap. VII. 14-25; with a general survey of Chapters III, IV, V, VI, VII, and VIII : followed by a brief commentary, in which the principles of the essay are applied /

Includes bibliographical references.

Diarii spiritualis partis 1ae vol.i,ii; pars 2a; partis 3ae vol.i,ii; pars 4a sive Diarium minus; partis 5ae vol.i,ii; pars 6a,7a [sectio i], ii,iv,v (in 4 vol.)

Vol.4 contains pt.4, 6, and 7, [sectio i], ii,iv,v. anal. in vol. IV, "pt.7, sectio 4,5."

Handbuch des schleswig-holsteinischen privatrechts. Bd. i-iv; v. abth. I.

Mode of access: Internet.

Chronica medii ævi : argumento generaliora, auctoritate celebriora, usu communiora, post Eusebium atque Hieronymum res secc. IV. V. et VI. exponentia. Tomus /

Signatures: *⁴ chi1 A-Y⁸ Z⁴ 2A².

Gai Iuli Caesaris De bello gallico commentariorum IV. V. /

Text in Latin.

Scriptores ecclesiastici minores saecvlorvm IV. V. VI.

fasc. I. Evagrii Altercatio legis inter Simonem Ivdaevm et Theophilvm Christianvm. Recensvit Edvardvs Bratke.

Maimonides Commentar zum Tractat Sanhedrin : Abschnitt IV-V : arabischer Urtext mit verbesserter hebraischer Uebersetzung, und Anmerkungen.

Thesis (doctoral)--Grossherzoglich Hessische Landesuniversitat zu Giessen.

Opere di Giambattista Vico, ordinate ed illustrate coll'analisi storica della mente di Vico in relazione alla scienza della civiltà

Half-title.

Chemistry of molecular and supramolecular structures of vanadium(IV) and dioxygen-bridged V(V) complexes incorporating tridentate hydrazone ligands

Four hydrazone ligands: 2-benzoylpyridine benzoyl hydrazone (HBPB), di-2-pyridyl ketone nicotinoyl hydrazone (HDKN), quinoline-2-carbaldehyde benzoyl hydrazone (HQCB), and quinoline-2-carbaldehyde nicotinoyl hydrazone (HQCN) and four of their complexes with vanadyl salts have been synthesized and characterized. Single crystals of HBPB and complexes [VO(BPB)(l2-O)]2 (1) and [VO(DKN)(l2-O)]2 ½H2O (2) were isolated and characterized by X-ray crystallography. Each of the complexes exhibits a binuclear structure where two vanadium(V) atoms are bridged by two oxygen atoms to form distorted octahedral structures within cis-N2O4 donor sets. In most complexes, the uninegative anions function as tridentate ligands, coordinating through the pyridyl- and azomethine-nitrogen atoms and enolic oxygen whereas in complex [VO(HQCN)(SO4)]SO4 4H2O (4) the ligand is coordinated in the keto form. Complexes [VO(QCB)( OMe)] 1.5H2O (3) and 4 are found to be EPR active and showed well-resolved axial anisotropy with two sets of eight line pattern

Synthesis, structure and solution chemistry of mixed-ligand oxovanadium(IV) and oxovanadium(V) complexes incorporating tridentate ONO donor hydrazone ligands

In the title family, the ONO donor ligands are the acetylhydrazones of salicylaidehyde (H2L1) and 2-hydroxyacetophenone (H2L2) (general abbreviation, H2L). The reaction of bis(acetylacetonato)oxovanadium(IV) with a mixture of tridentate H2L and a bidentate NN donor [e.g., 2,2'-bipyridine(bpy) or 1,10-phenanthroline(phen), hereafter B] ligands in equimolar ratio afforded the tetravalent complexes of the type [(VO)-O-IV(L)(B)]; complexes (1)-(4) whereas, if B is replaced by 8-hydroxyquinoline(Hhq) (which is a bidentate ON donor ligand), the above reaction mixture yielded the pentavalent complexes of the type [(VO)-O-V(L)(hq)]; complexes (5) and (6). Aerial oxygen is most likely the oxidant (for the oxidation of V-IV -> V-V) in the synthesis of pentavalent complexes (5) and (6). [(VO)-O-IV(L)(B)] complexes are one electron paramagnetic and display axial EPR spectra, while the [(VO)-O-V(L)(hq)] complexes are diamagnetic. The X-ray structure of [(VO)-O-V(L-2)(hq)] (6) indicates that H2L2 ligand is bonded with the vanadium meridionally in a tridentate dinegative fashion through its phenolic-O, enolic-O and imine-N atoms. The general bond length order is: oxo < phenolato < enolato. The V-O (enolato) bond is longer than V-O (phenolato) bond by similar to 0.07 angstrom and is identical with V-O (carboxylate) bond. H-1 NMR spectrum of (6) in CDCl3 solution indicates that the binding nature in the solid state is also retained in solution. Complexes (1)(4) display two ligand-field transitions in the visible region near 820 and 480 nm in DMF solution and exhibit irreversible oxidation peak near +0.60 V versus SCE in DMSO solution, while complexes (5) and (6) exhibit only LMCT band near 535 nm and display quasi-reversible one electron reduction peak near -0.10 V versus SCE in CH2Cl2 solution. The VO3+-VO2+ E-1/2 values shift considerably to more negative values when neutral NN donor is replaced by anionic ON donor species and it also provides better VO3+ binding via phenolato oxygen. For a given bidentate ligand, E-1/2 increases in the order: (L-2)(2-) < (L-1)(2-). (c) 2004 Elsevier B.V. All rights reserved.

Pactos sociales para una protección social más inclusiva: Experiencias, obstáculos y posibilidades en América Latina y Europa

Presentaciones de Alicia Bárcena y Christof Kersting.

Los officios de Sant Ambrosio, que tractan de las obras de virtud q[ue] guia[n] a la vida bienanue[n]turada / traduzidos de lengua latina en castellana ... por Diego Gracian ...

Capitulares grab. xil.

D. Hieronymi operum octauus tomus commentarios in Psalterium habet : accessit his Psalterium triplici lingua, Hebraica, Graeca, & Latina.

Imp. tomados del colofón en s7v