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Ring compounds, structure seven-membered

The enthalpy of fomation of two such species has been measured, namely the cyclopropane and cycloheptane derivatives. The difference between the values for these two species, both as solids, is 238.1 kJmol . Is this difference plausible Consider the difference between the enthalpies of formation of the parent cycloalkanes as solids, 194 kJ mol . The ca 44 kJ mol discrepancy between these two differences seems rather large. However, there are idiosyncracies associated with the enthalpies of formation of compounds with three-membered rings and almost nothing is known at all about the thermochemistry of compounds with seven-membered rings. Rather, we merely note that a seemingly well-defined synthesis of cycloheptyl methyl ketone was shown later to result in a mixture of methyl methylcyclohexyl ketones, and superelectrophilic carbonylation of cycloheptane resulted in the same products as methylcyclohexane, namely esters of 1-methylcyclohexanecarboxylic acid. The difference between the enthalpies of formation of the unsubstituted alicyclic hydrocarbons cycloheptane and methylcyclohexane as solids is 33 kJmol . This alternative structural assignment hereby corrects for most of the above 44 kJ mol discrepancy in the enthalpies of formation of the two oximes. More thermochemical measurements are needed, of oximes and cycloheptanes alike. [Pg.66]

Structures comprising Two Five-Membered Rings and One Seven-Membered Ring (5,5,7).—Azuleno[2,l-d]thiazoles [C3NS-CS-C7]. The reaction between the substituted azulenes (171 R = H or C02Et) and neutral or basic alumina gives the title compounds (172). ... [Pg.131]

Write a structural isomer of methylcyclooctane that has a nine-membered ring, a six-membered ring, and a seven-membered ring then, name all three compounds. [Pg.109]

Several spirocyclic compounds incorporating seven-membered rings have also been prepared by ring-closing metathesis. These molecules are important structural motifs that are found in a number of natural and unnatural products. A number of examples are illustrated in the paragraphs below. [Pg.541]

The NMR spectra of heterocyclic compounds with seven or more ring members are as diverse as the shape, size and degree of unsaturation of the compounds. NMR is perhaps the most important physical method to ascertain the structure, especially the conformational statics and dynamics, of large heterocycles. Proton-proton coupling constants provide a wealth of data on the shape of the molecules, while chemical shift data, heteroatom-proton coupling constants and heteronuclear spectra give information of the electronic structure. Details are found in Chapters 5.16-5.22. Some data on seven-membered rings are included in Table 10. [Pg.16]

Methyl-7-(trimethylsilyl)oxepin and 4-methyl-4//-l,2,4-triazole-3,5-dione as dienophile undergo a Diels-Alder reaction in which the 4,6-diene structure of the seven-membered ring react. Contrary to the aforementioned reactions, the primary adduct 12 is stable and does not rearrange to a carbonyl compound.222... [Pg.50]

X-ray structure analysis of compound 8a shows that the seven-membered ring is folded by... [Pg.367]

Benzopentathiepins are stable solids. Varacin, a cytotoxic metabolite, was isolated from a marine ascidian.398 The parent benzopentathiepin exhibits infrared absorptions at 1620, 1570, 1235 and 1020 cm" 1.399 X-ray structure analyses of benzopentathiepin and 6-methylbenzopen-talhicpin show that the seven-membered ring in both compounds is nonplanar and that it adopts a chair conformation. The S-S bond lengths are in the range 204-206 pm.400... [Pg.491]

As already mentioned, the macrocyclic ring can be further enhanced if the propylene moiety is substituted by a butylene group. Visible spectral data of a series of related compounds [Cu(L BF2)D]X 132 and the structural study of the derivative with D = H2O show that the seven-membered chelate ring influences the structure and other properties like electronic absorption of the copper(II) complex [193]. [Pg.38]

Following the first observation, eight substituted tropylium ions [94" ]-[98" ], [30 ], [34" ] and [35" ] (Scheme 1) were combined with Kuhn s carbanion [2 ] to make ionically dissociative hydrocarbons [94-2]-[98-2], [30-2], [34-2] and [35-2]. The structures of these hydrocarbons were determined as indicated in (23) on the basis of their and nmr spectra. Compounds [94-2], [95-2], [98-2] and [35-2] were mixtures of two positional isomers, in which [2 ] is connected to different positions of the seven-membered ring. Positions that formed a carbon-carbon bond with [2 ] are indicated by dots in Scheme 1. [Pg.192]

The zinc bis(tetraseleno) anion, [Zn(Se4)2]2-, has been crystallized with a number of cations, synthesized by a variety of methods, and its reactivity studied.581-584 The compound (hexaseleno) (tetraseleno)zinc (64) was synthesized from zinc acetate in the presence of lithium polyselenide and structurally characterized, demonstrating seven-membered and flve-membered ZnSen rings.585 Mixed donor neutral monomers have also been formed with imidazole A-donor ligands, ZnSe4 (A-methylimidazole)2.553... [Pg.1198]

The structure of the labile intermediate compound "Y" is uncertain. On the basis of its physical properties and chemical behaviour (which cannot be detailed here), possible formulations that were originally (485) considered included a six-membered bridged carbonyl-structure, as well as seven- or five-membered rings. The Italian group of workers (536) favoured the seven-membered ring-structure (CXVI) for the intermediate "Y", and 5-phenylguanamine structures (CXXI) for the final stable products. [Pg.56]

The basic chemical structure of the benzodiazepines consists of a benzene ring coupled to a seven-member heterocyclic structure containing two nitrogens (di-azepine) at positions 1 and 4 (Fig. 30.1). Of the 2,000 benzodiazepines that have been synthesized, approximately 15 clinically useful compounds are on the market in the United States (Table 30.1). [Pg.356]


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See also in sourсe #XX -- [ Pg.111 ]




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Seven-membered

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