Search results for "Amide"

Strong Ferromagnetic Coupling in Linear Mixed μ-Acetato, μ-Hydroxo Trinuclear Copper(II) Complexes withN-sulfonamide derivatives − Synthesis, Structu…

2002

Nicethamid‐Analoge, V Untersuchungen zur gehinderten internen Rotation bei N , N ‐Dimethylpyridinamiden

1975

Die Synthese von homologen, vinylogen und Kernalkylierten N,N-Dimethylnicotinamiden wird beschrieben und die Energiebarriere bei der gehinderten Rotation der Amidgruppe mittels 1H-NMR-Spektroskopie bestimmt. Nicethamide Analogues, V. Investigations of Hindered Internal Rotation in N,N-Dimethylpyridinamides The synthesis of homologue, vinylogue and ringalkylated N,N-dimethyl nicotinamides is described and the energy barrier of the hindered rotation of the amide group determined by means of 1H-n. m. r. spectroscopy.

( 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.

Preparation, Properties, and Reactivity of (Aminoferrocenyl)(ferrocenyl)carbene(pentacarbonyl)chromium(0) as Bulky Isolobal Trimetallo-amide

2015

Nucleophilic substitution of the ethoxy substituent in the Fischer carbene complex (ethoxy)(ferrocenyl)carbene(pentacarbonyl)chromium(0) (1) by ferrocenyl amide [Fc-NH]– [2-H]– gives the hetero trimetallic complex (aminoferrocenyl)(ferrocenyl)carbene (pentacarbonyl)chromium(0) (3). As the Cr(CO)5 fragment is isolobal to oxygen or sulfur 3 can be viewed as an isolobal metallo analogue to diferrocenylamide (Fc)(FcNH)C=O (4) and diferrocenylthioamide (Fc)(FcNH)C=S (5). The impact of the formal replacement of O/S by Cr(CO)5 in 3 is studied with respect to steric and electronic consequences as well as reactivity by spectroscopic, diffraction, electrochemical and theoretical methods.

Clathration effects on the interpenetration in the 2D (4,4) coordination polymer {[Fe(4,4 ′ -bipy)(dca) 2 ] · bt}

2004

Abstract A novel 2D polymer, {[Fe(4,4′-bipy)(dca)2] · bt}, (dca=dicyanamide, 4,4′-bipy=4,4′-bipyridine and bt=2,2′-bithiazoline) has been synthesized and characterized by X-ray crystallography. The structure reveals the formation of 2D (4,4) networks and intercalated bt uncoordinated ligands.

The first example of a hetero-tetranuclear [(VO)Gd](2) complex: synthesis, crystal structure and magnetic properties of [VOLGd(hfa)(2)CH(3)OH](2).2CH…

2005

A cyclic tetranuclear [VIVO–GdIII]2 complex with VO and Gd ions alternately arrayed, behaves, from the magnetic point of view, as two independent dinuclear entities each having a S = 4 ground state, as a consequence of an active and ferromagnetic VO–Gd interaction through the double phenoxo bridge and a magnetically inactive VO–Gd interaction through the amide bridge.

Syntheses and reactivity of aminobis(diorganylamino)phosphanes

1996

Aminobis(diorganylamino)phosphanes (R2N)2PNH2 (R = iPr, c-Hex, Ph) (2a–c), were obtained by treatment of the corresponding chlorobis(diorganylamino)phosphanes 1a–c with lithium amide in liquid ammonia. The transition metal phosphane complex (R2N)2(H2N)PNi(CO)3 (3) was prepared by reaction of 2a with tetracarbonylnickel. N-Complexation of 2a with trimethylalane affords the iminophosphorane-alane adduct (R2N)2HP=N(H)AlMe3 (4) by 1,2-H shift from the nitrogen to the phosphorus atom. The corresponding reaction with aluminium trichloride leads to the formation of the salt [(R2N)2HP=N(H)]2AlC12+[AlC14]− (5), in which two iminophosphorane moieties are linked by an AlCl2 bridge. Lithiation of 2a an…

Synthesis, crystal structures and magnetic properties of a P-stereogenic ortho-(4-amino-tempo)phosphinic amide radical and its CuII complex

2021

The synthesis of phosphinic amides containing one 4-amino-TEMPO substituent at the ortho position has been achieved through copper(I) catalyzed cross-coupling reactions of ortho-iodophosphinic amides with 4-amino-TEMPO. The method has been extended to the preparation of the first example of a P-stereogenic ortho-(4-amino-tempo)phosphinic amide radical 10. The reaction of 10 with Cu(hfac)2 afforded the P-stereogenic CuII complex 19. The crystal structure of both chiral compounds is reported. The molecular structure of 10 consists of a supramolecular zig-zag chain formed by intermolecular hydrogen bonds between the NH group of the phosphinic amide moiety and the nitroxide oxygen atom. In comp…

Synthesis and Characterization of Base Labile Poly(N-isopropylacrylamide) Networks Utilizing a Reactive Cross-Linker

2008

Topologically Controlled Interpolyelectrolyte Complexes

2008

The complexation of a cylindrical polyelectrolyte−brush−surfactant complex (PMMPSS−C12) and an oppositely, highly charged cylindrical polyelectrolyte−brush (PMMPEI−PEO) in dimethylformamide (DMF) l...