0000000000470829
AUTHOR
José Luis Serrano
Solid state conformational and theoretical study of complexes containing the (CxN)Pd moiety (CxN = 2-(phenylazo)phenyl-C,N and its derivatives)
Palladium complexes having the 2-(phenylazo)phenyl-C,N ligand exhibit a planar chelating ring with NN and N–C distances longer and shorter respectively than those found in trans-azobenzene. The ligand is not planar upon complexation, the mean angle between the phenyl ring and the chelating one found in the Cambridge Structural Database being of 45.6°. We have quantified and characterised the kind of distortion from planar coordination around metallic centers. The method employed makes use of two improper torsion angles, tetrahedral distortion being most frequently found in phenylazophenyl palladium complexes. Crystal structures of three succinimidate complexes having the title moiety are re…
Extended liquid-crystalline oligofluorenes with photo- and electroluminescence
In this paper we report the synthesis and characterization of a series of low-molecular weight light-emitting molecules based on short oligofluorene cores, from one to three 9,9-dioctylfluorene units, elongated at the 2- and 7-positions by means of promesogenic units. The effect of this structural modification on the mesomorphic properties, as well as on the optical and electrochemical properties, is studied. The possibility of using these molecules as emitters in light-emitting diodes (LEDs) and polarized photoluminescent layers has been explored.
Reactivity of the di-μ-hydroxo-complexes [{Pd(NN)}2(μ-OH)2][ClO4]2 (NN=bis(pyrazol-1-yl)alkanes) towards protic electrophiles. Hydration of coordinated nitriles at a palladium(II) site
Abstract The hydroxo-complexes [{Pd(μ-OH)(NN)}2][ClO4]2 (NN=bpzm:bis(pyrazol-1-yl) methane: a-compounds, bpzm*:bis(3,5-dimethylpyrazol-1-yl)methane; b-compounds) react with a wide variety of weak protic electrophiles H(LL) in a 1:2 molar ratio to give the mononuclear cationic palladium(II) derivatives of general formula [Pd(LL)(NN)][ClO4] [LL=2-pyridine-methoxo (OCH2-py) (1a,b); picolinate (pic) (2a,b); 8-hydroxiquinolinate (oxin) (3a,b)] or the dinuclear complexes [{Pd(NN)}2(μ-ox)][ClO4]2 [ox=oxalate: (4a,b)] and [{Pd(μ-LL)(NN)}2][ClO4]2 [LL=pyrazolate (pz) (5a,b); p-thiocresolate (SC6H4Me-p) (6a,b); triazolate (tz) (7b); thiophenolate (SPh) (8b)] when reacting with oxalic acid, azole…
Self-assembly of Clicked Star-Shaped Triazines into Functional Nanostructures
Two non‐amphiphilic star‐shaped 2,4,6‐tris(1,2,3‐triazol‐4‐yl)‐1,3,5‐triazines showing different behavior in terms of self‐assembly and luminescent properties are described. They aggregate in the liquid phase to form low‐dimensional nanostructures with a variety of morphologies, such as spherical particles, one‐hole hollow spheres, toroids, twisted fibers or helical nanotubes, just by varying the conditions of a straightforward reprecipitation method. Aggregation has an opposite effect concerning the fluorescent properties of the proposed compounds, either causing the enhancement or the quenching of the emission after the self‐assembly. Quantum chemical calculations have been also performed…
Reactivity Towards Acidic Protic Ligands of Cyclopalladated Di‐μ‐hydroxo Complexes
The dinuclear hydroxo complexes [{Pd(μ-OH)(C∧N)}2] [C∧N = 2-(2-pyridyl)phenyl (Phpy) (I), 7,8-benzoquinolyl (Bzq) (II) and 2-(2-oxazolinyl)phenyl (Phox) (III)] react in a 1:2 molar ratio with a wide variety of protic electrophiles H(L∧L) bearing different sets of donor atoms (L∧L = O∧O or O∧N) to give the mononuclear neutral palladium(II) derivatives with the general formula [Pd(L∧L)(C∧N)] [O∧O = salicylaldehydate (sal) (1), acetylacetonate (acac) (2) and benzoylacetonate (bzac) (3); O∧N = N-phenylsalicylaldiminate (N-Phsal) (4), N-p-chlorophenylsalicylaldiminate (N-pClPhsal) (5), 2-pyrrolecarbaldeydate (2-pcal) (6), 8-hydroxyquinolinate (oxin) (7)]. Structural characterisation of complexes…
Organometallic Nickel(II) Complexes Containing Thiolate and Dithiocarbamate Ligands
Synthesis and characterization of cyclometallated palladium(II) complexes with 2-(diphenylphosphino)benzaldehyde
New palladium(II) complexes containing 2-(diphenylphosphino)benzaldehyde a (Ph2P(o-C6H4CHO), displaying different coordination modes, have been synthesized in moderate to good yields (62–91%). The cyclometallated palladium(II) complexes [Pd(C^N)(Ph2 P(o-C6H4CHO)(Cl)] (1–4) in which a is P-monodentate have been prepared by reacting it with selected cyclometallated precursors containing bridging chlorides [Pd(C^N)(μ-Cl)]2 [C^N=2-phenylpyridine (Phpy), 7,8-benzoquinoline (Bzq), azobenzene (Phazo), and 2-phenyloxazoline (Phox), respectively]. A rigid P,O-chelating behavior of a, confirmed by the crystal structure determination of [Pd(Phox)(Ph2 P (o-C6H4CHO)][CF3SO3] (8), is observed in complexe…
Synthesis and characterization of new oxazoline-based palladacycles with bridging or terminal imidate ligands. Crystal structures of [{Pd(μ-dibromomaleimidate)(Phox)}2], [Pd(dibromomaleimidate)(Phox)(PPh3)] and [Pd(glutarimidate)(Phox)(PPh3)] (Phox=2-(2-oxazolinyl)phenyl))
Abstract The dinuclear hydroxo complex [{Pd(μ-OH)(Phox)}2] (I) (Phox = 2-(2-oxazolinyl)phenyl) reacts in a 1:2 molar ratio with several imidate ligands to yield new cyclometallated palladium complexes [{Pd(μ-NCO)(Phox)}2] containing asymmetric imidate –NCO– bridging units. [–NCO– = succinimidate (succ) (1), phtalimidate (phtal) (2), maleimidate (mal) (3), 2,3-dibromomaleimidate (2,3-diBrmal) (4) and glutarimidate (glut) (5)]. The reaction of these complexes with tertiary phosphines provides novel mononuclear N-bonded imidate derivatives of the general formula [Pd(imidate)(Phox)(PR3)] [R = Ph (a), 4-F–C6H4 (b) or CH2CH2CN (c)]. The new complexes were characterized by partial elemental analys…