Search results for "Derivative"

Photochemie des 1,3,5‐Tristyrylbenzols

1984

In Abhangigkeit von den Reaktionsbedingungen erhalt man bei der Belichtung der Titelverbindung 1 das Cyclophan 5, das Pyrenderivat 6 oder das polykondensierte aromatische System 9. Fur den neuen Cyclophantyp 5, bei dem zwei Benzolringe selbst wieder durch Ringe verbruckt sind, wurde eine Rontgenstrukturanalyse durchgefuhrt. Photochemistry of 1,3,5-Tristyrylbenzene Depending on the reaction conditions the irradiation of the title compound 1 yields the cyclophane 5, the pyrene derivative 6, or the polycondensed aromatic system 9. An X-ray analysis was performed for 5, representing a new type of cyclophane in which two benzene rings are bridged again by rings.

Zinn - Chalkogen - Heterocyclen. V. 2,2,3,3,5,5,6,6-Octamethyl-1.4-dithia-2,3,5,6-tetpastan-ninan, Darstellung und Zersetzung eines Zinnreichen Heter…

1977

Abstract The title compound can be regarded as a sulfur derivative of the corresponding organoditin compound arid contains -formally- tin in the oxidation state 3. It is prepared in analogy to tris (dimethyltinsulfide).

Cyclophosphazenes as versatile substrates in polymer chemistry

2004

In this article we present the synthesis of new cyclophosphazenes and their use as chain extenders, polymers compatibilizers, and monomers.

Synthesis and Electrochemical Reactivity of sigma-Bonded and N-Substituted Cobalt Porphycenes.

1998

The first synthesis and characterization of sigma-bonded and N-substituted cobalt porphycenes is reported. The investigated compounds are represented as (Pc)Co(R) and (N-CH(3)OEPc)CoCl, where R is CH(3) or C(6)H(5), Pc is the dianion of 2,3,6,7,12,13,16,17-octaethylporphycene (OEPc), 2,7,12,17-tetrapropylporphycene (TPrPc), or 2,7,12,17-tetraethyl-3,6,13,16-tetramethylporphycene (EtioPc), N-CH(3)OEPc is the monoanion of N-methyl-2,3,6,7,12,13,16,17-octaethylporphycene. Each sigma-bonded (Pc)Co(R) derivative can be reversibly reduced or oxidized by two electrons, but a slow migration of the sigma-bonded R group occurs following electrogeneration of [(Pc)Co(R)](+)()(*)() leading, as a final p…

Syntheses, Characterization, and Magnetic Studies of Copper(II) Complexes with the Ligand N,N,N′,N′-Tetrakis(2-pyridylmethyl)-1,3-benzenediamine (1,3…

2011

The copper(II) complexes [Cu4(1,3-tpbd)2(H2O)4(NO3)4]n(NO3)4n·13nH2O (1), [Cu4(1,3-tpbd)2(AsO4)(ClO4)3(H2O)](ClO4)2·2H2O·0.5CH3OH (2), [Cu4(1,3-tpbd)2(PO4)(ClO4)3(H2O)](ClO4)2·2H2O·0.5CH3OH (3), [C...

Formation and Reactivity of a Tantalocene Trihydride Containing an Aminoethyl‐Functionalised Ligand

2003

The complex [Cp*{C5H4(CH2CH2NMe2)}TaCl2] (1) was synthesised by reaction of the lithium salt LiC5H4(CH2CH2NMe2) with the tantalum compound [Cp*TaCl3(PMe3)]. Reduction of 1 with NaAl(H)2(OCH2CH2OMe)2 leads to the trihydride derivative [Cp*{C5H4(CH2CH2NMe2)}TaH3] (2). The oxidation of 2 in THF with ferrocenium ion leads to a cationic dihydride intermediate [Cp*{C5H4(CH2CH2NMe2)}TaH2]PF6 (3) with an intramolecular stabilization by the aminoethyl side-chain of the cyclopentadienyl ligand. The hemilabile character of the functionalised cyclopentadienyl ligand was checked by treating 3 with electron-donating ligands (e.g. phosphanes, sulfides, anions); in all cases, no displacement of the amino g…

Synthesis and Complexation of the Metalloligand {(η5-C5H5)[η5-C5Me3-1,2-(PPh2)2]TiCl2} (TiPHOS): The First Example of a 1,2-Bis(diphenylphosphanyl)ti…

2001

The reaction of lithium 1,2-bis(diphenylphosphanyl)trimethylcyclopentadienide (1) with CpTiCl3 leads to the formation of the titanocene diphosphane {(η5-C5H5)[η5-C5Me3-1,2-(PPh2)2]TiCl2} (TiPHOS, 2). This metalloligand reacts readily with (NBD)Cr(CO)4 and W(CO)5(THF) to give, in both cases, the bimetallic chelate complexes (TiPHOS)Cr(CO)4 (3) and (TiPHOS)W(CO)4 (4). The structure of 4 has been determined by X-ray diffraction. The synthesis of a new early-late heterobimetallic complex (TiPHOS)Rh(CO)Cl (5) is reported.

Influence of Xantphos Derivative Ligands on the Coordination in Their Copper(I) and Silver(I) Complexes

2019

Synthesis and Characterizations of Novel Isatin-s-Triazine Hydrazone Derivatives : X-ray Structure, Hirshfeld Analysis and DFT Calculations

2023

A novel series of isatin-s-triazine hydrazone derivatives has been synthesized and reported herein. The synthetic methodology involved the reaction of s-triazine hydrazine precursors with isatin derivatives in the presence of CH3COOH as a catalyst and EtOH as solvent to afford the corresponding target products 6a-e in high yields and purities. The characterization data obtained from elemental analysis, FT-IR, NMR (1H- and 13C-) were in full agreement with the expected structures. Furthermore, an X-ray single crystal diffraction study of one of the target s-triazine hydrazone derivatives, 6c confirmed the structure of the desired compounds. It crystallized in the triclinic crystal system and…

Structural and Spectroscopic Studies of the PCP-Bridged Heavy Chalcogen-Centered Monoanions [HC(PPh2E)(PPh2)]− (E = Se, Te) and [HC(PR2E)2]− (E = Se,…

2009

Selenium- and tellurium-containing bis(diphenylphosphinoyl)methane monoanions were prepared by oxidation of the anion [HC(PPh2)2]− with elemental chalcogens. The selenium-containing isopropyl derivative was synthesized by generating [H2C(PiPr2)2] via a reaction between [H2C(PCl2)2] and 4 equiv of iPrMgCl prior to in situ oxidation with selenium followed by deprotonation with LiNiPr2. The solid-state structures of the lithium salts of the monochalcogeno anions TMEDA·Li[HC(PPh2E)(PPh2)] (E = Se (Li7a), E = Te (Li7b)) and the dichalcogeno anions TMEDA·Li[HC(PR2Se)2] (R = Ph (Li8a), iPr (Li8c)) revealed five- and six-membered LiEPCP and LiSePCPSe rings, respectively. The homoleptic group 12 com…