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1,804 results

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Quoted phrases not found in phrase index: "1,2,5,6-dibenzonaphthalene", "1,2-benzphenanthrene"
Page 1
Carcinogenicity of methylchrysenes.
Hoffmann D, Bondinell WE, Wynder EL. Hoffmann D, et al. Science. 1974 Jan 18;183(4121):215-6. doi: 10.1126/science.183.4121.215. Science. 1974. PMID: 4808861
Methylchrysenes are present in tobacco smoke and are suspected to contribute to the tumorigenicity of this inhalant. Chrysene and the six isomeric methylchrysenes were obtained in high purity (99.9 percent); they were tested on mouse skin for tumor initiating activity and …
Methylchrysenes are present in tobacco smoke and are suspected to contribute to the tumorigenicity of this inhalant. Chrysene and the …
Chrysene-Based Blue Emitters.
Nathusius M, Ejlli B, Rominger F, Freudenberg J, Bunz UHF, Müllen K. Nathusius M, et al. Chemistry. 2020 Nov 26;26(66):15089-15093. doi: 10.1002/chem.202001808. Epub 2020 Oct 19. Chemistry. 2020. PMID: 32741022 Free PMC article.
Chrysene and its bisbenzannulated homologue, naphtho[2,3-c]tetraphene, were synthesized through a PtCl(2) -catalyzed cyclization of alkynes, which also furnished corresponding biaryls subsequent to a Glaser coupling reaction of the starting alkynes. The optoelectronic prop
Chrysene and its bisbenzannulated homologue, naphtho[2,3-c]tetraphene, were synthesized through a PtCl(2) -catalyzed cyclization of a
Chrysene.
[No authors listed] [No authors listed] IARC Monogr Eval Carcinog Risk Chem Hum. 1983 Dec;32:247-61. IARC Monogr Eval Carcinog Risk Chem Hum. 1983. PMID: 6586655 No abstract available.
Isolation and characterization of a newly chrysene-degrading Achromobacter aegrifaciens.
Lazzem A, Lekired A, Ouzari HI, Landoulsi A, Chatti A, El May A. Lazzem A, et al. Int Microbiol. 2024 Jun;27(3):857-869. doi: 10.1007/s10123-023-00435-0. Epub 2023 Oct 18. Int Microbiol. 2024. PMID: 37851202
In our study, we isolated a potential chrysene-degrading bacteria from crude oil-contaminated seawater (Bizerte, Tunisia). Based on 16SrRNA analysis, the isolate S5 was identified as Achromobacter aegrifaciens. ...Confirmation was obtained via gas chromatography-mass spect …
In our study, we isolated a potential chrysene-degrading bacteria from crude oil-contaminated seawater (Bizerte, Tunisia). Based on 1 …
Radical-promoted Stone-Wales rearrangements.
Alder RW, Harvey JN. Alder RW, et al. J Am Chem Soc. 2004 Mar 3;126(8):2490-4. doi: 10.1021/ja039389r. J Am Chem Soc. 2004. PMID: 14982458
The mechanism of the known Stone-Wales rearrangement of bifluorenylidene to dibenzo[g,p]chrysene is assessed with the aid of B3LYP/6-31G(d) density functional calculations, and it is shown that a radical-promoted mechanism involving a sequence of homoallyl-cyclopropylcarbi …
The mechanism of the known Stone-Wales rearrangement of bifluorenylidene to dibenzo[g,p]chrysene is assessed with the aid of B3LYP/6- …
Chrysene contribution to bronchial asthma: Activation of TRPA1 disrupts bronchial epithelial barrier via ERK pathway.
Zhou X, Zhao X, Dong H, Gao Y. Zhou X, et al. Ecotoxicol Environ Saf. 2024 Nov 1;286:117095. doi: 10.1016/j.ecoenv.2024.117095. Epub 2024 Oct 11. Ecotoxicol Environ Saf. 2024. PMID: 39395376 Free article.
Chrysene induced airway epithelial barrier dysfunction primarily through TRPA1 instead of transient receptor potential vanilloid 1. ...Coexposure to chrysene and HDM increased TRPA1 expression. The animal test verified that the TRPA1 inhibitor HC030031 could suppres
Chrysene induced airway epithelial barrier dysfunction primarily through TRPA1 instead of transient receptor potential vanilloid 1. .
3,6,9,12-Tetrasubstituted chrysenes: synthesis, photophysical properties, and application as blue fluorescent OLED.
Wu TL, Chou HH, Huang PY, Cheng CH, Liu RS. Wu TL, et al. J Org Chem. 2014 Jan 3;79(1):267-74. doi: 10.1021/jo402429q. Epub 2013 Dec 5. J Org Chem. 2014. PMID: 24295385
A short synthesis of unsubstituted chrysene is described to provide a cheap source of this compound. This chrysene was used to prepare 3,6,9,12-tetrabromochrysene, which was subsequently transformed into various 3,6,9,12-tetrasubstituted chrysenes bearing four aryl, …
A short synthesis of unsubstituted chrysene is described to provide a cheap source of this compound. This chrysene was used to …
Tetraphenylethylene-Arylamine Derivatives as Hole Transporting Materials for Perovskite Solar Cells.
Zhang X, Liu X, Ghadari R, Li M, Zhou Z, Ding Y, Cai M, Dai S. Zhang X, et al. ACS Appl Mater Interfaces. 2021 Mar 17;13(10):12322-12330. doi: 10.1021/acsami.1c01606. Epub 2021 Mar 8. ACS Appl Mater Interfaces. 2021. PMID: 33683113
A series of hole transporting materials (HTMs) with fused tetraphenylethylene cores (9,9'-bifluorenylidene and dibenzo[g,p]chrysene) as well as different substitution positions of arylamine side arms has been designed and synthesized. ...When used in perovskite solar cells …
A series of hole transporting materials (HTMs) with fused tetraphenylethylene cores (9,9'-bifluorenylidene and dibenzo[g,p]chrysene) …
An Efficient Electron Donor for Conjugated Microporous Polymer Photocatalysts with High Photocatalytic Hydrogen Evolution Activity.
Han C, Xiang S, Ge M, Xie P, Zhang C, Jiang JX. Han C, et al. Small. 2022 Jul;18(28):e2202072. doi: 10.1002/smll.202202072. Epub 2022 Jun 10. Small. 2022. PMID: 35689304
Herein, two dibenzo[b,d]thiophene-S,S-dioxide (BTDO) containing CMP photocatalysts using tetraphenylethylene (TPE) or dibenzo[g,p]chrysene (DBC) as the electron donor to investigate the influence of the geometry of electron donor on the photocatalytic activity are design a …
Herein, two dibenzo[b,d]thiophene-S,S-dioxide (BTDO) containing CMP photocatalysts using tetraphenylethylene (TPE) or dibenzo[g,p]chrysen
Synthesis of Chrysene-Based Nanographenes by a Successive APEX Reaction.
Nakashige Y, Nakatsuji H, Matsushima K, Murakami K, Ito H, Itami K. Nakashige Y, et al. Precis Chem. 2025 Apr 18;3(9):535-540. doi: 10.1021/prechem.5c00032. eCollection 2025 Sep 22. Precis Chem. 2025. PMID: 41001094 Free PMC article.
Chrysene-based nanographenes (ChrNGs), despite their relatively small structures, have been reported to exhibit low highest occupied molecular orbital (HOMO)-lowest unoccupied molecular orbital (LUMO) energy gaps and strong long-wavelength fluorescence, making them attract
Chrysene-based nanographenes (ChrNGs), despite their relatively small structures, have been reported to exhibit low highest occupied
1,804 results