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71.
Diorganomorpholinometalates of Gallium and Indium – Monomer‐Dimer‐Equilibrium in Solution The reaction of Li[N(CH2CH2)2O] (LiMorpholinate; Li(Morph)) with Me2GaCl and Me2InCl gives by salt‐elimination the diorganoamidometalates Me2M(Morph) ( M = Ga: 1 ; M = In: 2 ), respectively. 1 and 2 were characterized by NMR and vibrational spectroscopy as well as by X‐ray structure determinations. According to this, centrosymmetrical dimers are present in the solid state while a monomer‐dimer equilibrium was assumed for the THF‐solution. Cryoscopic molecular weight determinations confirmed our assumptions. 相似文献
72.
Dianjie Ma Yasuaki Okamoto Takahiro Kumamaru Etsuro Iwamoto 《Analytica chimica acta》1999,390(1-3):201-206
Tungsten-coated non-pyrolytic graphite (NPG), pyrolytic graphite (PG) and pyrolytic L'vov platform graphite (PPG) tubes were prepared, and their analytical performances were compared. The coating process simply involved injecting 100 μl of a sodium tungstate solution (0.01 mol l−1) into each graphite tube, followed by heating according to a temperature programme similar to an atomisation cycle for the determination of gallium. This procedure for coating was repeated at least 12, 25, and 7 times towards NPG, PG, and PPG tubes, respectively. Among these tubes, the tungsten-coated PPG tube showed excellent performance for the determination of gallium. By combined use of a chemical modifier such as aluminium(III) or nickel(II) a detection limit (3σ) of 6 pg and sensitivity (1% absorption) of 3–4 pg were achieved. The practical potential of the proposed technique was demonstrated for the determination of gallium in several samples of alloys and fresh water. 相似文献
73.
Hubert Schmidbaur 《Angewandte Chemie (International ed. in English)》1985,24(11):893-904
Arene complexes of main-group metals were, until recently, rare species—in contrast to the now classical, analogous complexes of transition metals. In systematic investigations, it has been possible to prepare and structurally characterize arene complexes of the univalent elements gallium, indium, and thallium, which directly follow the d-block elements in the periodic table. This new type of compound is characterized by centric (η6) coordination of the metal to the arene; both mono- and bis(arene) complexes are known. The interaction can be explained by the perfect agreement between the HOMO/LUMO symmetry of the arene and of the low-valent metal. The electronic states of the nd10(n + 1)s2 configuration, which are partially modified by relativistic effects, play a particularly important role. The relationship to the few known complexes of the neighboring elements (SnII, PbII) becomes plausible via the isoelectronic principle. The arene/GaI, InI, TlI systems are of potential significance as homogeneous reducing agents and as agents for the activation of aromatic compounds, the purification of metals, and the separation of metals from nonaqueous media. 相似文献
74.
Synthesis,Single Crystal Growth and Crystal Structure of Ta7Cu10Ga34 – a 8 × 4 × 2 Super Structure of CsCl
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Single crystals of Ta7Cu10Ga34 were grown from the elements in a Cu/Ga melt. Ta7Cu10Ga34 represents the first ternary compound of the system Ta/Cu/Ga. The crystal structure (Cmmm, oC102, Z = 2, a = 23.803(1), b = 12.2087(4), c = 5.7487(2) Å, 1291 refl. 78 parameters, R1 = 0.037, wR2 = 0.070). The crystal structure is characterized by rods of pentagonal prisms MGa10, which are alternatingly occupied by Ta and Cu. Four of these rods are connected to columns running in direction (001). These columns are linked by cubic units TaGa8, CuGa8, and GaGa8. According to the characteristic structural elements and the size of the unit cell Ta7Cu10Ga34 represents a 8 × 4 × 2 super structure of CsCl or bcc. With respect to the underlying CsCl structure the formula can be written as [Ta7Cu10Ga2□13]Ga32, i.e. a cubic primitive packing of 32 Ga atoms with Ta, Cu, and Ga in cubic voids and 13 vacancies. The pentagonal‐prismatic coordination of Ta and Cu can formally be obtained from the cubic primitive packing of Ga atoms by a 45° rotation of a part of the Ga8 cubes. There is a close similarity to the binary compounds Ta8Ga41 and Ta2–xGa5+x. The first one is also related to a CsCl‐like structure, the latter one contains rods of pentagonal prisms, which form the same columns. There are also relations to the ternaries V2Cu3Ga8 and V11Cu9Ga46, whose cubic structures are more or less complex variants of CsCl. 相似文献
75.
Synthesis and Characterization of GaIII,YIII, and LuIII Complexes with Etifenin and Analogues 下载免费PDF全文
Michel Pfeifer‐Leeg Gergely Szabó Zsolt Baranyai Tobias Niksch Wolfgang Weigand Martin Freesmeyer 《无机化学与普通化学杂志》2016,642(6):486-491
Complexes of etifenin ( 1a ), disofenin ( 1b ), and mebrofenin ( 1c ) with GaIII, YIII, and LuIII were synthesized and characterized by NMR spectroscopy and UV/Vis spectroscopy. Stability and protonation constants of the complexes of 1a were determined by potentiometry and distribution diagrams were calculated. It was shown that the YIII and LuIII species are most stable as bis chelates at higher pH, whereas the GaIII complex degrades at pH < 4.5. 相似文献
76.
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78.
F. Schaller W. Schwarz H.-D. Hausen K. W. Klinkhammer J. Weidlein 《无机化学与普通化学杂志》1997,623(9):1455-1466
Base-free Tris(trimethylsilyl)methyl Derivatives of Lithium, Aluminium, Gallium, and Indium Base-free LiR* (R*=-C(SiMe3)3) has been prepared from R*Cl and Li-metal in toluene at 85?90°C and used to synthesize the metallanes R*MMe2 with M = Al, Ga and In, respectively. The NMR (1H, 13C, 29Si) and the vibrational spectra of these trisyl compounds have been discussed. AlCl3 and LiR*(ratio 1 : 1) forms the metallate metallate Li[R*AlCl3]. The triclinic unit cell (space group P1 ) consists of a centrosymmetric assoziate, formed by four Li[R*AlCl3]- units with Al? Cl…?Li bridges, two pairs of Li-atoms differing in their chlorine-coordination and two disordered toluene molecules, inserted in the crystal lattice (R1wR2 =0,0444/0,1072). The reaction of GaCl3 with LiR* (I :1) gives the unusual sesquichloride (R*Ga(Cl1,33)Me0,67)3 in moderate yield. The X-ray structure determination shows a Ga3Cl3-skeleton with chairconformation and disordered, terminal gallium ligands (R1/wR2= 0,0646/0,2270). 相似文献
79.
Dariusz Basiak Wanda Ziemkowska Paweł Socha Łukasz Dobrzycki Zbigniew Ochal Edyta Pindelska 《Journal of Coordination Chemistry》2017,70(9):1528-1535
2-Mercapto-1,3-benzothiazole (mbztH) may act as a chelating or bridging ligand. In this study, reactions of mbztH with Me3Ga and Me3In were examined. The products were characterized by NMR spectroscopy, elemental analyses, melting point, and molecular weight determinations. Formation of mononuclear chelating complexes Me2M(mbzt) (M = Ga, In) was observed in solutions. Crystallization of Me2M(mbzt) yielded uncommon non-symmetrical dinuclear complexes Me4M2(mbzt)2, in which one metal is bonded to two sulfurs and the other to two nitrogens. 相似文献
80.
Synthesis and Structures of Gallium‐β‐Diketiminate Complexes: Isolation of a Dinuclear Gallium(II) Complex 下载免费PDF全文
The sterically demanding β‐diketiminate ligand Ldmp [Ldmp = HC{(CMe)N(dmp)}2, dmp = C6H3‐2,6‐Me2] was used to stabilize various gallium complexes in the formal oxidation states +II and +III. The reaction of in situ generated [LdmpLi] with gallium chloride affords [LdmpGaCl2] ( 1 ), which was used as starting complex to synthesize a variety of gallium(III) compounds [LdmpGaX2] [X = F ( 2 ), I ( 3 ), H ( 4 ), and Me ( 5 )]. Synthesis of the dinuclear complex [LdmpGaI]2 ( 6 ), with gallium in the formal oxidation state +II was accomplished by converting “GaI” with in situ generated [LdmpLi] in toluene. All compounds were characterized by elemental analyses, NMR spectroscopy, LIFDI‐TOF‐MS, and single‐crystal X‐ray diffraction. Additionally DFT calculations were performed for analysis of the bonding in 6 . 相似文献