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High-temperature intramolecular cyclization of N, N-dialkyl-N'-(4-substituted-2-ethynylphenyl)triazenes provides under neutral conditions both 6-substituted cinnolines and 5-substituted isoindazoles in moderate to excellent yields. 相似文献
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D P Egolf B T Haley V D Larson 《The Journal of the Acoustical Society of America》1986,79(5):1592-1602
In the literature there are several references which imply that various parts of a hearing aid are sources of constant volume velocity. Reported herein are the findings of an investigation of the validity of such statements. A computer scheme, referenced elsewhere, for modeling in situ hearing aids was utilized to test the constant-volume-velocity hypothesis. In particular, capabilities of the receiver, ear hook, and earmold tip to deliver constant volume velocity were investigated via a computer. To facilitate such an investigation, a universal receiver/earmold model was created. This model was broken down into "source" and "load"at three locations: the receive output, output of the ear hook, and medial tip of the earmold. At each location comparisons were made between computed values of source and load impedance. The constant-volume-velocity hypothesis was assumed to be valid for those cases where source impedance was much, much greater than load impedance. Plots of such impedances show that, for the cases investigated, this rarely occurred, except over certain frequency bands. With the exception of in-the-ear hearing aids, these results appear to contradict inferences made in the literature about the constant-volume-velocity nature of hearing aids. 相似文献
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N. F. Haley 《Journal of heterocyclic chemistry》1977,14(7):1245-1247
The reaction of 2- or 4-methyl-2,6-diphenylpyrylium perchlorate with tetracyanoethylene (TCNE) in pyridine gives 2- or 4-(2,3,3-tricyanopropylidene)-2,6-diphenylpyran in good yield. Similar results are obtained from 2- or 4-methyl-2,6-diphenylthiapyrylium and 4-methylflavylium perchlorates. In one case a stable charge-transfer salt is isolated from the reaction of a methylene base and TCNE. The reaction mechanism of dye formation is discussed. 相似文献
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Kimball DB Haley MM Mitchell RH Ward TR Bandyopadhyay S Williams RV Armantrout JR 《The Journal of organic chemistry》2002,67(25):8798-8811
The synthesis and study of dehydrobenzoannulene (DBA)-dimethyldihydropyrene (DDP) hybrids as models for the investigation of aromaticity in weakly diatropic systems is reported. Three new monofused DBA-DDP hybrids have been synthesized, and their NMR spectra are discussed with regard to quantifying the aromaticity remaining in multibenzene-fused DBAs. Nucleus-independent chemical shifts, determined at a series of locations for each compound, bond lengths, and (1)H and (13)C NMR chemical shifts were calculated and used to probe the aromaticity of these hybrids. Systems where more than one annulene/DBA is fused to the DDP core have also been obtained, and their potential use in photoinduced isomerization applications is discussed. 相似文献
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