Title:
PHENACENE COMPOUND, METHOD FOR PRODUCING PHENACENE COMPOUND, AND ORGANIC LIGHT-EMITTING DIODE
Document Type and Number:
WIPO Patent Application WO/2017/065219
Kind Code:
A1
Abstract:
A phenacene compound represented by general formula (1). In general formula (1), R1, R2, R3, R4, R5, R6, R7, R8, R9, and R10 each independently represent a hydrogen atom or a group represented by general formula (2), and any one of R3, R5, and R6 is a group represented by general formula (2). R9 and R10, together with the carbon atoms to which R9 and R10 are bonded, may bond to each other to form a condensed ring. In general formula (2), * indicates the bonding position with a compound represented by general formula (1). X indicates a halogen group, and Y1 represents an aryl group or heteroaryl group.
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Inventors:
YAMAJI MINORU (JP)
Application Number:
PCT/JP2016/080392
Publication Date:
April 20, 2017
Filing Date:
October 13, 2016
Export Citation:
Assignee:
NAT UNIV CORP GUNMA UNIV (JP)
International Classes:
C07F5/02; C07C45/67; C07C45/77; C07C49/784; C07C49/92; C09K11/06; H01L51/50
Foreign References:
| JP2015178474A | 2015-10-08 | |||
| JPS61176537A | 1986-08-08 |
Other References:
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ADAMS J. CHRISTOPHER ET AL.: "Friedel-crafts reactions in room temperature ionic liquids", CHEMICAL COMMUNICATIONS, 1998, pages 2097 - 2098, XP002172928
BALO C. ET AL.: "1H NMR spectra of monosubstituted phenanthrenes", SPECTROCHIMICA ACTA, vol. 50 A, no. 5, 1994, pages 937 - 940, XP055378189
OTA E.: "Some aromatic reactions using aluminum chloride-rich molten salts", PROCEEDINGS- ELECTROCHEMICAL SOCIETY, vol. 87, no. 7, 1987, pages 1002 - 1010
BACHMANN W. E. ET AL.: "Phenanthrene derivatives. V. Beckmann rearrangement of the oximes of acetylphenanthrenes and benzoylphenanthrenes", JOURNAL OF THE AMERICA CHEMSICAL SOCIETY, vol. 58, 1936, pages 2097 - 2101
BACHMANN W. E. ET AL.: "The preparation of phenanthryl amines and phenanthryl halides", JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, vol. 58, May 1936 (1936-05-01), pages 857 - 858, XP055378196
BUU-HOÏ N. P. ET AL.: "Les réactions de friedel-crafts d'acylation des hydrocarbures aromatiques polycycliques. II. Effets de solvant dans l'acétylation du phénanthrène", BULLETIN DE LA SOCIÉTÉ CHIMIQUE DE FRANCE, 1966, pages 180 - 184
CHANDRASEKHAR SOSALE ET AL.: "Chloral hydrate as a water carrier for the efficient deprotection of acetals, dithioacetals, and tetrahydropyranyl ethers in organic solvents", SYNTHETIC COMMUNICATIONS, vol. 44, no. 13, 2014, pages 1904 - 1913, XP055378197
FU WAI CHUNG ET AL.: "Exploiting aryl mesylates and tosylates in catalytic mono-alpha-arylation of aryl- and heteroarylketones", ORGANIC LETTERS, vol. 18, no. 8, 15 April 2016 (2016-04-15), pages 1872 - 1875, XP055378200
LEVY LIRON ET AL.: "Reversible Friedel-crafts acylations of phenanthrene: rearrangements of acetylphenanthrenes", LETTERS IN ORGANIC CHEMISTRY, vol. 4, no. 5, 2007, pages 314 - 318
ADAMS J. CHRISTOPHER ET AL.: "Friedel-crafts reactions in room temperature ionic liquids", CHEMICAL COMMUNICATIONS, 1998, pages 2097 - 2098, XP002172928
BALO C. ET AL.: "1H NMR spectra of monosubstituted phenanthrenes", SPECTROCHIMICA ACTA, vol. 50 A, no. 5, 1994, pages 937 - 940, XP055378189
OTA E.: "Some aromatic reactions using aluminum chloride-rich molten salts", PROCEEDINGS- ELECTROCHEMICAL SOCIETY, vol. 87, no. 7, 1987, pages 1002 - 1010
BACHMANN W. E. ET AL.: "Phenanthrene derivatives. V. Beckmann rearrangement of the oximes of acetylphenanthrenes and benzoylphenanthrenes", JOURNAL OF THE AMERICA CHEMSICAL SOCIETY, vol. 58, 1936, pages 2097 - 2101
BACHMANN W. E. ET AL.: "The preparation of phenanthryl amines and phenanthryl halides", JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, vol. 58, May 1936 (1936-05-01), pages 857 - 858, XP055378196
BUU-HOÏ N. P. ET AL.: "Les réactions de friedel-crafts d'acylation des hydrocarbures aromatiques polycycliques. II. Effets de solvant dans l'acétylation du phénanthrène", BULLETIN DE LA SOCIÉTÉ CHIMIQUE DE FRANCE, 1966, pages 180 - 184
CHANDRASEKHAR SOSALE ET AL.: "Chloral hydrate as a water carrier for the efficient deprotection of acetals, dithioacetals, and tetrahydropyranyl ethers in organic solvents", SYNTHETIC COMMUNICATIONS, vol. 44, no. 13, 2014, pages 1904 - 1913, XP055378197
FU WAI CHUNG ET AL.: "Exploiting aryl mesylates and tosylates in catalytic mono-alpha-arylation of aryl- and heteroarylketones", ORGANIC LETTERS, vol. 18, no. 8, 15 April 2016 (2016-04-15), pages 1872 - 1875, XP055378200
Attorney, Agent or Firm:
NAKAJIMA, Jun et al. (JP)
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