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2 edition of Intramolecular coordination in organotin chemistry = found in the catalog.

Intramolecular coordination in organotin chemistry =

Johann To ns Barthold Heinrich Jastrzebski

Intramolecular coordination in organotin chemistry =

Intramoleculaire coo rdinatie in de Organotinchemie : (met een samenvatting in het Nederlands).

by Johann To ns Barthold Heinrich Jastrzebski

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Published by J. T. B. H. Jastrzebski in [Utrecht] .
Written in English


ID Numbers
Open LibraryOL13967096M

This book provides a review of cyclometalation reactions and organometallic intramolecular-coordination five-membered ring products, eBook Packages Chemistry and Materials Science Chemistry and Material Science (R0) Print ISBN ;. Coordination Chemistry is a collection of invited lectures presented at the 20th International Conference on Coordination Chemistry held in Calcutta, India, on December , , and organized by the International Union of Pure and Applied Chemistry in cooperation with India's National Science Academy and the Department of Science & Technology.

high coordination ability of tin, especially its ability to participate either in weak or strong intra or intermolecular coordination [6], has given organotin (IV) chemistry wide recognition. Tin compounds have a fascinating solution and solid phase chemistry [7]. The coordination characteristics of. Five novel tin Schiff base complexes with histidine analogues (derived from the condensation reaction between L-histidine and 3,5-di-tert-butylhydroxybenzaldehyde) have been synthesized and terization has been completed by IR and high-resolution mass spectroscopy, 1D and 2D solution NMR (1 H, 13 C and Sn), as well as solid state Sn NMR.

Among these, Schiff base organotin complexes have received much attention, as such ligands and their metal complexes are reported to exhibit bactericidal and antitumor activities [5, 6]. The coordination chemistry of tin is extensive with various geometries and coordination numbers known for both inorganic and organometallic complexes. Chapter 9, end and Chapter


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Intramolecular coordination in organotin chemistry = by Johann To ns Barthold Heinrich Jastrzebski Download PDF EPUB FB2

Intramolecular Coordination in Organotin Chemistry The Occurrence of intramolecular Sn-N coordination has been unambiguously deduced from the observation that the H NMR spectrum of the C-chiral compound SnBr,Me[C,H,CH(Me)NMe,-(S)-2],at 25 "C shows two resonances for the NMe, by: Comparative assessment of weak intramolecular coordinations at tin in functionalized mono-organotin trichlorides and mono-organotrialkynyltins by multinuclear solution NMR.

Journal of Organometallic Chemistry(2), DOI: /SX(98)Cited by: Organotin compounds or stannanes are chemical compounds based on tin with hydrocarbon substituents. Organotin chemistry is part of the wider field of organometallic first organotin compound was diethyltin diiodide ((C 2 H 5) 2 SnI 2), discovered by Edward Frankland in The area grew rapidly in the s, especially after the discovery of the Grignard reagents.

Organotin chemistry. [Iwao Omae] Book: All Authors / Contributors: Iwao Omae. Find more information about: ISBN: Tetrahedral organotin compounds and other higher-coordination compounds. Organotin intramolecular-coordination compounds.

Spectroscopic Investigations. Sn NMR spectroscopy. Sn Mossbauer. New Organoantimony Compounds with Intramolecular N→Sb Coordination, Oana-Alina BUMBU, Inorganic and Organomercury Compounds with Intramolecular Coordination and Compounds with Au−M−C (M = Hg, Te) Fragment, Adina Olimpia ROTAR, Studies on Hypervalent Organotin Compounds, Albert Paul SORAN.

trends for organotin coordination compounds hav e been well. in the intramolecular pentacoordinate, ketiminotin trichloride. Book Review: Organotin Chemistry, Synthesis and. If the purely electrostatic interaction26 between the ortho-substituent and the solvent donor atom in the solvated species is ignored, it is possible to suggest that where intramolecular coordination of the univalent organotin and -lead groups occurs in the compounds investigated the electron-accepting ability of the metal orbital involved in.

The 1H, 13C, 15N and Sn NMR study of the intramolecular Sn–N interaction in tri- and tetraorganotin compounds containing the chiral 2-(4-isopropyloxazolinyl)phenyl ligand. Journal of Molecular Structure(), The field of organotin chemistry has a long history that started sincewhen Frankland isolated a specimen of diethyltin diiodide [1].

InLowich reported on the reaction of alkyl halides with a tin-sodium alloy giving alkyltin compounds [2]. This last publication is usually considered to represent the beginning of organotin chemistry. A series of ten aryl-triazole-functionalized boranes bearing BMes 2-groups and capable of forming intramolecular five-membered N→B-coordinated heterocycles, has been prepared by 1,3-dipolar onically diverse substituents ranging from 4-NMe 2-phenyl (4-NMe 2) and 4-OMe-phenyl (4-OMe) to 4-cyanophenyl (4-CN), 4-nitrophenyl (4-NO 2) and pentafluorophenyl (C 6 F 5).

Intramolecular Coordination in Organotin Chemistry DSpace/Manakin Repository. Intramolecular Coordination in Organotin Chemistry Koten, G. van; Jastrzebski, J.T.B.H. () Advances in organometallic chemistry, vol pp. - (Article) Download/Full Text. Open Access version via Utrecht University Repository.

Insights into the Intramolecular Donor Stabilisation of Organostannylene Palladium and Platinum Complexes: Syntheses, Structures and DFT Calculations † Michael Wagner Lehrstuhl für Anorganische Chemie II, Technische Universität Dortmund, Dortmund (Germany), Fax: (+49) ‐‐ Alkyl, silyl, and phosphane ligands - Classical ligands in nonclassical bonding modes.

Braunstein, N. Boag,Int. Engl.,40, Key Words. Sn NMR data are reported for organotin compounds containing potentially C,N‐chelating ligands capable of forming five‐ or six‐membered chelate rings.

The Sn chemical shifts of divalent organotin compounds containing such a ligand are found at relatively high frequency. Intramolecular coordination in tetraorganotin compounds has little influence on their Sn chemical shifts.

Significant attention has been given to organotin(IV) dithiocabamate compounds in recent times. This is due to their ability to stabilize specific stereochemistry in their complexes, and their diverse application in agriculture, biology, catalysis and as single source precursors for tin sulfide nanoparticles.

These complexes have good coordination chemistry, stability and diverse molecular. A study was made of the absorption bands In the –cm−1 region of the spectra of o-carbonylcontaining phenols, and their phenylmercury and triethyltin derivatives, in polar and nonpolar solvents.

It has been shown that the carbonyl groups in these compounds coordinate with the phenylmercury and triethyltin groups. The stability of chelate rings with formyl groups is.

Schiff bases are the most widely used versatile ligands, able to coordinate many elements and to stabilize them in various oxidation states. Recently, this class of compounds has been employed as models for biological systems, and in control of stereochemistry in six-coordinate transition metal complexes.

Intramolecular Coordination in Organotin Chemistry () Pagina-navigatie: Main; Save publication. Save as MODS; Export to Mendeley; Save as EndNote. Chapter One Introduction History. The first organotin compound was prepared over years ago.

Inin a paper devoted largely to the reaction which occurred when ethyl iodide and zinc were heated together in a sealed tube, Frankland says: "In conclusion, I will describe, very briefly, the behaviour of iodide of ethyl in contact with several other metals, at elevated temperatures.

A wide variety of stabilized carbanions have been found to participate as nucleophiles in intramolecular Michael-type conjugate additions to in situ generated nitrosoalkenes to form bridged carbocyclic systems.

The vinylnitroso platforms for these cyclizations have been prepared via two key steps involving ring-closing metathesis of vinyl chlorides and regioselective conversion of vinyl.

Download PDF: Sorry, we are unable to provide the full text but you may find it at the following location(s): :8 (external link).A new tetranuclear organotin sulfide cage [(RSn IV) 4 (μ-S) 6]2CHCl 3 4H 2 O is designed and synthesized by exploiting intramolecular coordination using 2-phenylazophenyl (N → Sn) as an organic substituent on tin.

Resistive Molecular Memory Device is fabricated for the very first time using Organotin based complex with the ON/OFF ratio of 10 studies suggested that 2.Explore the latest full-text research PDFs, articles, conference papers, preprints and more on MAIN GROUP CHEMISTRY. Find methods information, sources, references or conduct a literature review on.