Ethylene bridges

Tricyclic Antidepressants. Imipramine [50-49-7] (32), which was the first tricycHc antidepressant to be developed, is one of many useful psychoactive compounds derived from systematic molecular modifications of the antihistamine prometha2ine [60-87-7] (see Histamine and histamine antagonists). The sulfur atom of prometha2ine was replaced with an ethylene bridge and the dimethylamino group attached to an / -propyl group, rather than to an isopropyl one, of the side chain. The actual synthesis of (32) is typical of the compounds in this class (37). 

The 3,5-bis(trifluoromethyl)pyrazolate analog [Ir(cod)(/x-3,5-(CF3)2pz)]2 does not enter into oxidative addition with iodine, methyl iodide, or acetylenes. The mixture of pyrazolate and 3,5-bis(trifluoromethyl)pyrazolate gives [(rj -codllrf/x-pz)(/L-3,5-(CF3)2pz)Ir(rj -cod)], which reacts with bis(trifluoromethyl)acetylene in a peculiar manner [83JCS(CC)580], producing 145, where 3,5-bis(trifluoromethyl) pyrazolate is replaced by the ethylene bridge and the rj -coordination mode of one of the cod ligands is converted into the rj -allylic mode. 

The indoloquinolizidine alkaloid Villagorgin B (360) was isolated from the Gorgonian Villagorgia rubra collected in New Caledonia (Scheme 108). The positive charge of the molecule was deduced from the chemical shifts of the C-6 and C-5 ethylene bridge. However, only one NH group was detectable in NMR in DMSO-Jg (93TL7773). Additional heteroaromatic... 

One of the two carbon atoms of the ethylene bridge of the antidepressants may be replaced by oxygen. Attachment of the side chain via the olefinic linkage found in amytriptyline affords antidepressants with a biologic profile similar to the carbocy-clic prototype. 

Property Ethylene-bridged zirconocenes Ziegler-Natta... 

Ethylene-bridged bis-indenyl zirconocene dichloride-methylalu-moxane system. 

Similarly, efficient tetracyclization (MeAlCl2-promoted) of the bis-allylic silane/ bis-epoxide 97 constitutes the key step in the synthesis of (+)-a-onocerin. In this case, because of the presence of the bis-allylic silane group, a double bis-annula-tion occurs, with the formation of the ethylene-bridge linked bis-decalin system present in the target compound (Scheme 8.26) [46],... 

Liquid Crystals Containing Azo, Azoxy, Azine, Azomethine Units or an Ethylene Bridge... 

In this section, we will report on the X-ray structure analyses of some mesogenic compounds containing an ethylene bridge. The crystal data and the phase sequences of the investigated compounds are summarised in Table 17. 

Table 17. Crystal data and phase sequences of mesogenic compounds containing an ethylene bridge and some derivatives...

Isomers are, of course, possible when the equatorial ligand lacks a plane of symmetry, as in the corrinoids [see (HI)]. All the acetamide side chains project to one side of the corrin ring, which we shall call the upper side, and all the propionamide side chains and the nucleotide side chain to the lower side. Isomers are then theoretically possible whenever the two axial ligands are different, and their existence has been shown experimentally for corrinoids where one axial ligand is CN , Me, or Et and the other is H2O or is absent [for further details see Section 8.2 of ref. (136)]. Salen and BAE also show minor deviations from planarity due to the bending of the two halves (mentioned above in Section II,B,2) and to torsion about the C—C bonds in the ethylene bridge (see references in Table I), but these are not expected to give rise to separable isomers. 

Silicas used in this study were FSM-16 (BET surface area 950m g pore diameter 2.7 nm), ethylene bridged... 

Introduction of an ethylene bridge between the maso-carbon atom and one of the diaminophenyl groups of a triarylmethane-type phthalide results in a considerable bathochromic shift, thus producing color formers exhibiting absorption in the near infrared region of the electromagnetic spectrum. 

The experiment took 11 min, and the spectrum shows quite clearly the correlation signals for the acetal 5 cross peaks between the methyl and methylene signals from the ethyl group and between the magnetically non-equivalent protons of the ethylene bridge. CH correlation experiments can easily also be carried out, even though in the case of the two acetals 4 and 5 they require between two and three hours ... 

Another possible source of modification of the HBI optical properties arises from cis-trans (or, more properly, Z-E) isomerization around its exocyclic ethylene bridge (dihedral angle x as depicted in Fig. 3a) [74, 75]. The absorption spectrum of trans HBI in different solvents is red-shifted by 5-10 nm compared to that of the cis conformation [76]. While the trans conformation is thermodynamically unfavorable and contributes only a minor population at room temperature, cis-trans isomerization seems to take place regardless of the chromophore ionization state, and involves a relatively low energy barrier of about 50 kJ/mol [75], a value that appears significantly lower than initially predicted from quantum mechanics [77, 78]. 

As shown in Table 1, a remarkable variety of alkene complexes bearing metal centers in a low oxidation state have been isolated and their structures have been determined by X-ray analysis. All the C-C bond distances in olefins coordinated to early transition metals at low oxidation states are more or less elongated compared to free ethylene. These structural data, together with those from NMR studies [14], indicate a major contribution of the metallacyclo-propane structure (2), a fact which is also supported by calculation studies [15]. In the case of ethylene bridging two metal centers such as [ Cp2ZrX 2(iu-f/-C2H4)] (3), the M-C bond could be characterized as a er-bond and there is a little contribution from the / -ethylene canonical structure [16-18]. 

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