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Novel oxo-bridged blue luminescent organoaluminum complexes: Al4(CH3)6(mu3-O)2(dpa)2 and Al3(7-azain)4(OCH(CF3)2) 2(CH3)(mu3-O) (dpa = deprotonated Di-2-pyridylamine, 7-azain = deprotonated 7-azaindole)

Two novel blue luminescent organoaluminum complexes Al4(CH3)6(mu3-O) 2(dpa)2 (1) and Al3(7-azain)4-(OCH(CF3)2) 2(CH3)(mu3-O) (2) (dpa = deprotonated di-2-pyridylamine, 7-azain = deprotonated 7-azaindole) have been synthesized and characterized structurally. The unusual stability of these compounds is attributed to the presence of the triply-bridging oxo ligand.

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The reactivity of five-coordinate Ru(II) (1,4-bis(diphenylphosphino)butane) complexes with the N-donor ligands: Ammonia, pyridine, 4-substituted pyridines, 2,2?-bipyridine, bis(o-pyridyl)amine, 1,10-phenanthroline, 4,7-diphenylphenanthroline and ethylenediamine

A series of Ru(II) (1,4-bis(diphenylphosphino)butane)(L)2complexes was synthesized from [RuCl2(dppb)]2(mu-dppb) or RuCl2(dppb)-(PPh3); dppb=Ph2P(CH2)4PPh2, L=NH3, pyridine (py), 4-aminopyridine (4-NH2py), 4-cyanopyridine (4-CNpy), 4-dimethylaminopyridine (4-Me2Npy), 4-methylpyridine (4-Mepy), 4-phenylpyridine (4-Phpy), 4-vinylpyridine (4-Vpy) and N-methylimidazole (MeIm), and L2=2,2?-bipyridine (bipy), bis(o-pyridyl)amine (bpa), 1,10-phenanthroline (phen),4,7-diphenylphenanthroline (or bathophenanthroline, batho) and ethylenediamine (en). The complexes were characterized by elemental analysis, cyclic voltammetry, UV-Vis, NMR and IR spectroscopies. The structures of trans-RuCl2(dppb)(py)2 (3), cis-RuCl2(dppb)(bipy) (4) and cis-RuCl2(dppb)(phen) (5) were established by X-ray crystallographic analyses. Crystals of trans-3, cis-4 ¡¤ CH2Cl2 and cis-5 ¡¤ solvate are all monoclinic, space group P21/c, with Z=4; a=12.946(2), b=14.204(3), c=18.439(4) A, beta=90.08(2) for trans-3; a=10.694(6), b=18.485(6), c=18.632(7) A, beta= 90.26(3) for cis-4 ¡¤ CH2Cl2; a=17.094(1), b=9.923(2), c=21.905(2) A, beta=98.883(6) for cis-5 ¡¤ solvate. The structures were solved by the heavy atom Patterson method and were refined by full-matrix least-squares procedures to R=0.069, 0.071 and 0.036 (Rw=0.069, 0.076 and 0.039) for 1957, 4165 and 4824 reflections with I ? 3sigma(I), respectively.

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Tetrahydropyran – Wikipedia,
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Can You Really Do Chemisty Experiments About 2,3,4,6-Tetra-o-acetyl-D-glucopyranose

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NIS/TFA: a general method for hydrolyzing thioglycosides

A variety of thioglycosides are chemoselectively hydrolyzed to the corresponding 1-hydroxy glycosides using equimolar amounts of NIS/TFA as promoter systems.

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Tetrahydropyran – Wikipedia,
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Efficient method for the one-pot azidation of alcohols using bis(p-nitrophenyl) phosphorazidate

The direct stereoselective conversion of various alcohols and hexopyranoses into the corresponding alkyl azides and glycosyl azides, respectively, is efficiently accomplished by using bis(p-nitrophenyl) phosphorazidate and DBU.

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Tetrahydropyran – Wikipedia,
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The structure and magnetic properties of a 3D pillared-layer polymer and two helical chains constructed from flexible ligands

Three novel coordination polymers of CoII and CuII with flexible ligands, namely [Co(oba)(dpa)]n (1), [Cu(oba)(dpa)]n (2) and [Cu(oba)(bpy)1/2]n (3) [H2oba = 4,4?-oxybis(benzoic acid), dpa = 2,2?-dipyridylamine, bpy = 4,4?-bipyridine] were synthesized by hydrothermal reactions and characterized by single-crystal X-ray diffraction, thermogravimetric analyses, elemental analysis and IR spectroscopy. X-ray diffraction analysis reveals that complexes 1 and 2 are isostructural. In complexes 1 and 2, the CoII and CuII ions are linked by flexible oba ligands to form 1D helical chain. These chains are further assembled into 3D supramolecular edifice via aromatic pi-pi stacking interactions and intermolecular hydrogen bonding. The CuII ions in complex 3 are linked by the carboxylate groups oba to form an eight-membered ring chains, the connectivity between the corner-shared eight-membered ring chains are further bridged by the bent oba ligands to produce 2D helical layer containing the right-handed helical chains. Furthermore, the adjacent helical layers are connected by bpy pillars to form a novel 3D framework with an unprecedented topology of (315¡¤420¡¤58¡¤62). The magnetic properties of complexes 1-3 have also been investigated.

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Tetrahydropyran – Wikipedia,
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A novel bonding mode of a deprotonated synanti 2,2?-dipyridylamine ligand to dimethyl aluminium and dimethyl gallium. Synthesis, characterization and X-ray crystal structure of Me2Ga(DPA) (DPA = 2,2?-dipyridylamine)

The reaction of 2,2?-dipyridylamine with R3M (R = CH3, M = Ga, Al) gave the Lewis acid-base adducts Me2Ga(dpa) and Me2Al(dpa) (where dpa is 2,2?dipyridylamide). X-ray analysis showed an unusual structure of dpa- in the formation of a new anti-anti complex Me2Ga(dpa) with extremely short bond distances Ga-N(1) [1.976(3) A] and Ga-N(2) [1.978(3) A]. The gallium atom is in a tetrahedral environment, coordinated to the deprotonated chelating ligand and two methyl groups. The bond distances N(3)-C(5) [1.345(4) A] and N(3)-C(6) [1.347(4) A] are almost identical. The bond angle N(1)-Ga-N(2) [92.0(1)] is 17 smaller than, and C(12)-Ga-N(1) [109.5(2)] is almost equal to, normal tetrahedral angles. These adducts are much less air- and moisture-sensitive than the metal trialkyl. The compounds were characterized by elemental analysis, NMR and mass spectroscopy. The conformation of the dipyridylamide ligand in the bidentate chelate complex is significantly different from that observed for other dipyridylamine complexes. Copyright

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Tetrahydropyran – Wikipedia,
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Ruthenium-catalysed cross metathesis binding of functionalized olefins to polystyrene resin via a novel allylsilyl linker suitable for electrophilic cleavage

1% Divinylbenzene-crosslinked allyldimethylsilyl polystyrene 1 undergoes highly efficient ruthenium-catalysed cross-metathesis with functionalized terminal olefins and allows electrophilic cleavage of the resulting functionalized allylsilane.

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Generation of near-enantiopure alpha-alkyl alpha-formyl alpha-hydroxy ketones/esters and their interception with ethoxycarbonylmethylenetriphenylphosphorane

Two protocols for the generation of the (R)-enantiomers of alpha-alkyl alpha- formyl alpha-hydoxy ketones/esters in states of high enantiomeric purity are developed; the formyl functions of such compounds undergo Wittig condensations with ethoxycarbonylmethylenetriphenylphosphorane in dimethyl sulfoxide to afford the corresponding alkenes with high (E)- stereoselectivities and with e.e.s of 91-99%.

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N-Nitroso and C-Nitro Derivatives from Di-(2-pyridyl)amine and Butyl Nitrite

The reaction between di-(2-pyridyl)amine and butyl nitrite produced N-nitrosodi-(2-pyridyl)amine, (5-nitro-2-pyridyl)-2-pyridylamine and (3-nitro-2-pyridyl)-2-pyridylamine of which the likely conformations are evinced from spectral data.Structural elucidation of N-nitrosodi-(2-pyridyl)amine in the solid state by X-ray diffraction excluded any substantial contribution of the rings to resonance structures.

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Tetrahydropyran – Wikipedia,
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New type of single Chain magnet: Pseudo-one-dimensional chain of high-spin Co(II) Exhibiting ferromagnetic intrachain interactions

Two new six-coordinated high-spin Co(II) complexes have been synthesized through the reactions of Co(II) salts with dipyridylamine (dpamH) and 5-nitro-salicylaldehyde (5-NO2-saloH) or 3-methoxy-salicylaldehyde (3-OCH3-saloH) under argon atmosphere: [Co(dpamH)2(5- NO2-salo)]NO3 (1) and [Co(dpamH)2(3-OCH 3-salo)]NO3¡¤1.3 EtOH¡¤0.4H2O (2). According to the crystal packing of compound 1, two coordination cations are linked with two nitrate anions into a cyclic dimeric arrangement via N-H…O and C-H…O hydrogen bonds. In turn, these dimers are assembled into (100) layers through pi-pi stacking interactions between inversion-center related pyridine rings of the dpamH ligands. The crystal packing of compound 2 reveals a 1D assembly consisting solely from the coordination cations, which is formed by pi-pi stacking interactions between pyridine rings of one of the dpamH along the [010] and another 1D assembly of the coordination cations and nitrate anions through the N-H…O hydrogen-bonding interactions along the [001] direction. All complexes were magnetically characterized, and a new approximation method was used to fit the magnetic susceptibility data in the whole temperature range 2-300 K on the basis of an empirical expression which allows the treatment of each cobalt(II) ion in axial symmetry as an effective spin Seff = 1/ 2. In zero-field, dynamic magnetic susceptibility measurements show slow magnetic relaxation below 5.5 K for compound 2. The slow dynamics may originate from the motion of broad domain walls and is characterized by an Arrhenius law with a single energy barrier Deltar/kB = 55(1) K for the [10-1488 Hz] frequency range. In order to reveal the importance of the crystal packing in the SCM behavior, a gentle heating process to 180 C was carried out to remove the solvent molecules. The system, after heating, undergoes a major but not complete collapse of the network retaining to a small percentage its SCM character.

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Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics