Search results for "HeLa"
showing 10 items of 738 documents
Synthesis, Reactivity, and X-ray Crystallographic Characterization of Mono-, Di-, and Tetranuclear Palladium(II)-Metalated Species
2001
The reactivity of the tetranuclear metallated palladium compound (Pd[mu 2-(C6H4)PPh2]Br)4 (1) with different ligands has been investigated with the aim of evaluating the influence of the entering ligand on the nature of the reaction products. The results confirmed the ability of the ligand [(C6H4)PPh2]- to expand a bridging [mu 2-] or a chelating [eta 2-] coordination mode, depending on the auxiliary ligands present in the complex. Bulky phosphines stabilize mononuclear species of formula (Pd[eta 2-(C6H4)PPh2]Br[P]), with a four-atom metallocycle, while small phosphines give dinuclear compounds. The molecular structures of three different metalated palladium compounds have been determined b…
Low-Dimensional 3d–4f Complexes Assembled by Low-Spin [FeIII(phen)(CN)4]− Anions
2013
The synthesis, crystal structure, and magnetic properties of four new mixed 3d-4f complexes with formulas [{FeIII(phen)(CN)4} 4Gd2 III(bpym)(NO3) 2(H2O)4]·2CH3CN· 2H2O}n (1), [{FeIII(phen)(CN)4} 4Tb2 III(bpym)(H2O) 8]·(NO3)2·2CH3CN} n (2), [{FeIII(phen)(CN)4}4Sm III(bpym)(NO3)2(H2O) 5]·2CH3CN}n (3), and [{Fe III(phen)(CN)4}2Pr2 III(bpym)(NO3)4(H2O) 2]n (4) (phen = 1,10-phenanthroline and bpym = 2,2′-bipyrimidine) are discussed here. Compounds 1-3 are isomorphous and their structure consists of neutral ladder-like motifs where the rungs are made up by bpym-bridged dilanthanide(III) cations and the rods are defined by [Fe(phen)(CN)4]- units adopting a bis-monodentate coordination mode through…
Organometallic complexes with biological molecules: XII. Solid-state and solution studies on dialkyltin(IV)- and trialkyltin(IV)-thiaminepyrophosphat…
1999
Dialkyltin(IV) and trialkyltin(IV) derivatives of the coenzyme thiaminepyrophosphate (H2TPP) have been synthesized with general formula R2Sn(HTPP)2·nH2O (Alk = Me, n = 2; Alk = Bu, n = 4) and R3SnHTPP·nH2O (R=Me, n = 2; R = Bu, n = 1), respectively. The solid-state structure of the complexes has been investigated through infrared and Mossbauer spectroscopy. The infrared data suggest the involvement of only phosphate oxygen atoms in the coordination of both dialkyl- and trialkyl-tin(IV) moieties, with phosphate anions behaving as monoanionic bidentate bridging or chelating groups, with the tin(IV) involved in six- and five-fold coordination geometries, respectively, in R2Sn(HTPP)2·nH2O (R = …
Chiral Self‐Sorting of trans ‐Chelating Chiral Ligands upon Formation of Pd II Complexes (Eur. J. Inorg. Chem. 15/2014)
2014
Chiral Self-Sorting of trans-Chelating Chiral Ligands upon Formation of PdII Complexes
2014
Invited for the cover of this issue is the group of Arne Lutzen at the University of Bonn, Germany. The cover image shows two dissymmetric bis(3-pyridyl) ligands based on a planar chiral pseudo-ortho-disubstituted [2.2]paracyclophane scaffold. Upon forming a mononuclear [ML2] complex with palladium(II) ions, these ligands act in a trans-chelating manner and undergo complete chiral self-sorting.
( E )‐ und ( Z )‐Enole von β‐Ketocarbonsäureamiden
1990
(E)- and (Z)-Enols of β-Ketocarboxylic Acid Amides Reaction of dimesitoyldiazomethane (1) with ammonia (3a), primary and secondary amines (3b – o and 3p – v, respectively) leads to the completely enolized amides 4a – v. Besides the chelated Z configuration the unusual E isomer exists in the most cases, too. The Z/E distribution in the equilibrium depends on the steric and electronic effects present in the amide group CONR2R3 and on the solvent.
Cavitands incorporating a Lewis acid dinickel chelate function as receptors for halide anions.
2015
The halide binding properties of the cavitand [Ni2(L(Me2H4))](2+) (4) are reported. Cavitand 4 exhibits a chelating N3Ni(μ-S)2NiN3 moiety with two square-pyramidal Ni(II)N3S2 units situated in an anion binding pocket of ∼4 Å diameter formed by the organic backbone of the (L(Me2H4))(2-) macrocycle. The receptor reacts with fluoride, chloride (in MeCN/MeOH), and bromide (in MeCN) ions to afford an isostructural series of halogenido-bridged complexes [Ni2(L(Me2H4))(μ-Hal)](+) (Hal = F(-) (5), Cl(-) (6), and Br(-) (7)) featuring a N3Ni(μ-S)2(μ-Hal)NiN3 core structure. No reaction occurs with iodide or other polyatomic anions (ClO4(-), NO3(-), HCO3(-), H2PO4(-), HSO4(-), SO4(2-)). The binding ev…
Structural diversity within analogous compounds: syntheses and studies of M(SCH2CH2NH2)Cl (M = Zn, Cd, Hg).
2006
The novel complexes [Zn(L)Cl] (1), [Cd(L)Cl] (2), [Hg(L)Cl] (3), {[Hg(L)Cl]·NaOH·2H 2 O} (3·NaOH·2H 2 O), and {[Hg 3 (HL) 2 Cl 6 ]·2H 2 O} (4) (L = -SCH 2 CH 2 NH 2 ) were prepared and investigated by means of IR spectroscopy and single-crystal X-ray diffraction. The crystal structures of 1, 2, and 3·NaOH·2H 2 O show chelating N,S-coordination of the cysteaminate ligand, bridging S, and terminally coordinating Cl. Apart from these common features, the coordination geometries and modes of intermolecular association are different. 1 forms a cyclic tetramer with a Zn 4 S 4 ring, and 3·NaOH·2H 2 O contains one-dimensional [Hg(L)Cl] n chains with S-bridged Hg atoms. Zn and Hg atoms in 1 and 3·Na…
The tris(hexasulphido)platinate(IV) ion: Seven-membered chelate rings
1988
Le sel complexe [[(C 6 H 5 ) 4 P] 2 Pt(S 6 ) 3 ] a l'etat cristallin est prepare a partir de [N(C 2 H 5 ) 4 ] 2 PtS 17 ou (NH 4 ) 2 PtS 17 •H 2 O en solution dans l'acetone. Caracterisation structurale et configuration geometrique de l'anion Pt(S 6 ) 3 2−