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1

Li, Peng-Peng, Li Zhao, Ji-Xing Zhao, Zhao-Bin Zhu, Fei Wang та Qin-Qin An. "Synthesis and crystal structure of bis{1-(((4-(1-(hydroxyimino)ethyl)phenyl)imino)methyl)naphthalen-2-olato-κ2O,N}copper(II), C38H30CuN4O4". Zeitschrift für Kristallographie - New Crystal Structures 232, № 6 (2017): 889–90. http://dx.doi.org/10.1515/ncrs-2017-0044.

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AbstractC38H30CuN4O4, triclinic, P1̅ (no. 2), a = 8.3882(7) Å, b = 8.5024(9) Å, c = 11.3649(15) Å, α = 89.960(10)°, β = 69.689(10)°, γ = 80.269(8)°, Z = 1, V = 747.73(15) Å3, Rgt(F) = 0.0701, wRref(F2) = 0.1308, T = 294.68(10) K.
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2

Zang, Kai-Kai, Xiao Xiao, Li-Qiang Chen, et al. "Distinct Function of Estrogen Receptors in the Rodent Anterior Cingulate Cortex in Pain-related Aversion." Anesthesiology 133, no. 1 (2020): 165–84. http://dx.doi.org/10.1097/aln.0000000000003324.

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Background Brain-derived estrogen is implicated in pain-related aversion; however, which estrogen receptors mediate this effect remains unclear. This study hypothesized that the different estrogen receptors in the rostral anterior cingulate cortex play distinct roles in pain-related aversion. Methods Formalin-induced conditioned place avoidance and place escape/avoidance paradigms were used to evaluate pain-related aversion in rodents. Immunohistochemistry and Western blotting were used to detect estrogen receptor expression. Patch-clamp recordings were used to examine N-methyl-d-aspartate–med
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3

Ma, Jin-Xia, Qing-Lin Li, Peng-Peng Li, Ji-Xing Zhao та Li Zhao. "Crystal structure of bis{5-methoxy-2-((E)-((4-((E)-1-(methoxyimino)ethyl)phenyl)imino)methyl)phenolato-κ2N,O}nickel(II), C34H34N4NiO6". Zeitschrift für Kristallographie - New Crystal Structures 233, № 5 (2018): 767–69. http://dx.doi.org/10.1515/ncrs-2017-0379.

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AbstractC34H34N4NiO6, monoclinic, P21/c (no. 14), a = 10.5538(5) Å, b = 6.1691(2) Å, c = 24.2831(9) Å, β = 100.519(4)°, Z = 2, V = 1554.43(11) Å3, Rgt(F) = 0.0402, wRref(F2) = 0.0973, T = 294.39(10) K.
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4

Zhang, Zi-Yang, Zhen-Zhong Huang, Yang Pan, and Cheng Song. "New transparent and thermally stable cardo poly(ether imide)s derived from 10,10-bis[4-(4-amino-2-pyridinoxy)phenyl]-9(10H)-anthrone." High Performance Polymers 32, no. 5 (2019): 483–93. http://dx.doi.org/10.1177/0954008319883005.

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A new diamine bearing flexible ether, rigid pyridine, and bulky anthrone pendent group, 10,10-bis[4-(4-amino-2-pyridinoxy)phenyl]-9(10 H)-anthrone (BAPPA), was prepared in three steps from anthrone. BAPPA was reacted with six conventional aromatic dianhydrides in N, N-dimethylacetamide (DMAc) to form the corresponding new poly(ether imide)s (PEIs) via the poly(ether amic acid) (PEAA) precursors with inherent viscosities ranging from 0.85 dL g−1 to 1.26 dL g−1 and thermal imidization. All the PEAAs could be cast from DMAc solution and thermally converted into transparent, flexible, and tough PE
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5

Krečmerová, Marcela, Hubert Hřebabecký, Milena Masojídková, and Antonín Holý. "Synthesis of 5-Phenyl-2(1H)-pyrimidinone Nucleosides." Collection of Czechoslovak Chemical Communications 61, no. 3 (1996): 458–77. http://dx.doi.org/10.1135/cccc19960458.

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Reaction of 2-phenyltrimethinium salt 1 with thiourea and subsequent reaction with chloroacetic acid afforded 5-phenyl-2(1H)-pyrimidinone (3). Its silyl derivative 4 was condensed with 1-O-acetyl-2,3,5-tri-O-benzoyl-D-ribofuranose under catalysis with tin tetrachloride or trimethylsilyl trifluoromethanesulfonate to give protected nucleoside 5 together with 5',O6-cyclo-5-phenyl-1,3-bis- (β-D-ribofuranosyl)-6-hydroxy-5,6-dihydro-2(1H,3H)-pyrimidinone (7). The greatest amounts of 7 were formed with the latter catalyst. Nucleosidation of the silyl derivative 4 with protected methyl 2-deoxy-D-ribof
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6

Zhou, Yu-Ting, Shou-Ri Sheng, Chuan-Chao Tang, Cheng Song, Zhen-Zhong Huang, and Xiao-Ling Liu. "Preparation and characterization of novel soluble polyarylates derived from 9,9-bis[4-(4-chloroformylphenoxy)phenyl]xanthene with various bisphenols." High Performance Polymers 30, no. 10 (2017): 1203–9. http://dx.doi.org/10.1177/0954008317744869.

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A series of new polyarylates bearing cardo xanthene groups were synthesized by phase-transfer-catalyzed interfacial polycondensation of 9,9-bis[4-(4-chloroformylphenoxy)phenyl]xanthene with various bisphenols containing the isopropylidene, hexafluoroisopropylidene, 1-phenylethylidene, diphenylmethane, cyclohexane, and xanthene structures. High-molecular-weight polyarylates with number-average molecular weight and polydispersity index in the range of 30,100–35,300 and 1.82–2.17, respectively, exhibited high glass transition temperatures ranged from 226°C to 261°C, and their 10% weight loss temp
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7

Luo, Yi-Sheng, Qiu-Ying Wang, Xue-Chun Mao, and Shou-Ri Sheng. "Synthesis and characterization of new cardo poly(ether amide)s containing 9(10H)-anthrone units." High Performance Polymers 32, no. 9 (2020): 1001–9. http://dx.doi.org/10.1177/0954008320918922.

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A new aromatic diamine, 10,10-bis[4-(4-aminophenoxy)phenyl]-9(10 H)-anthrone (BAPA) has been synthesized from anthrone via three-step procedure. Direct phosphorylation polycondensation of BAPA with various aromatic dicarboxylic acids produced a series of cardo poly(ether amide)s with inherent viscosities of 0.97–1.29 dL g−1. All the polymers were readily soluble in polar solvents such as N-methyl-2-pyrrolidone, N, N-dimethylacetamide (DMAc), and pyridine at room temperature, and afforded transparent, strong, and flexible films upon casting from DMAc solvent. The resulting poly(ether amide)s ha
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8

Ghorab, Mostafa M., Mansour S. Al-Said, and Reem K. Arafa. "Design, Synthesis and Potential Anti-Proliferative Activity of Some Novel 4-Aminoquinoline Derivatives." Acta Pharmaceutica 64, no. 3 (2014): 285–97. http://dx.doi.org/10.2478/acph-2014-0030.

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Abstract Novel nineteen compounds based on a 4-aminoquinoline scaffold were designed and synthesized as potential antiproliferative agents. The new compounds were N-substituted at the 4-position by aryl or heteroaryl (1-9), quinolin- 3-yl (10), 2-methylquinolin-3-yl (11), thiazol-2-yl (12), and dapsone moieties (13, 14 and 18). Bis-compounds 15, 16 and 19 were also synthesized to assess their biological activity. All the newly synthesized comounds were tested for in vitro antiproliferative activity against the MCF-7 breast cancer cell line. Seventeen of the novel compounds showed higher activi
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9

Weni, Mustika, Mega Safithri, and Djarot Sasongko Hami Seno. "Molecular Docking of Active Compounds Piper crocatum on the A-Glucosidase Enzyme as Antidiabetic." Indonesian Journal of Pharmaceutical Science and Technology 7, no. 2 (2020): 64. http://dx.doi.org/10.24198/ijpst.v7i2.21120.

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Ethanol extract of Piper crocatum leaves has inhibitory activity of α-glucosidase enzyme. Ethyl acetate fraction from Piper crocatum leaves has the highest antioxidant activity. Previous research has provided information that the ethyl acetate fraction of Piper crocatum leaves has an inhibition of α-glucosidase containing 6XO32ZSP1D, Ethyl L-serinate hydrochloride compound, Schisandrin B compound, Columbin compound, 4- (4-methoxy-phenylamino) -2 compound, 3-dihydro-1H-4a, 9-diazacyclopenta (b) fluorine-10-carbonitrile, compound 6-Amino-4- [3- (benzyloxy) phenyl] -3-tert-butyl-2,4-dihydropyrano
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10

Bertolasi, V., P. Gilli, V. Ferretti, and G. Gilli. "Intermolecular N-H...O Hydrogen Bonding Assisted by Resonance. II. Self Assembly of Hydrogen-Bonded Secondary Enaminones in Supramolecular Catemers." Acta Crystallographica Section B Structural Science 54, no. 1 (1998): 50–65. http://dx.doi.org/10.1107/s0108768197008677.

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The crystal structures of 15 compounds containing the 2-en-3-amino-1-one heterodienic system and forming intermolecular N—H...O hydrogen bonds assisted by resonance (RAHB) are reported: (1) 3-phenylamino-2-cyclohexen-1-one; (2) 3-(4-methoxyphenylamino)-2-cyclohexen-1-one; (3) 3-(4-chlorophenylamino)-2-cyclohexen-1-one; (4) 3-(4-methoxyphenylamino)-2-methyl-2-cyclohexen-1-one; (5) 3-(4-methoxyphenylamino)-5-methyl-2-cyclohexen-1-one; (6) 3-isopropylamino-5,5-dimethyl-2-cyclohexen-1-one; (7) 3-phenylamino-5,5-dimethyl-2-cyclohexen-1-one; (8) 3-(3-methoxyphenylamino)-5,5-dimethyl-2-cyclohexen-1-o
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11

Herberhold, Max, Christian Köhler, Volker Tröbs, and Bernd Wrackmeyer. "Tri(Terf-Butyl)plumbyl-phosphanes, Synthesis and Multinuclear Magnetic Resonance." Zeitschrift für Naturforschung B 55, no. 10 (2000): 939–45. http://dx.doi.org/10.1515/znb-2000-1008.

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AbstractThe reaction of tri(tert-butyl)plumbyl-lithium (1) with various phosphorus chlorides was studied. With diphenyl- and amino(phenyl)phosphorus chlorides the formation of hexa(tertbutyl) diplumbane (2) and tetraphenyldiphosphane (3) or the respective 1,2-bis(am ino)-1,2-diphenyl- diphosphanes [e. g. 5: amino = PhCH2(tBu)N] was dominant. The presence of at least one tert-butyl group at the phosphorus atom gave access to tri(tert-butyl)plumbyl-di(tert-butyl) phosphane (4) and to tri(tert-butyl)plumbyl-amino(tert-butyl)phosphanes [amino = tBu(H)N (6), Me(Ph)N (7), PhCH2(Me)N (8), PhCH2(tBu)N
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12

McGlinchey, Michael J., and Kirill Nikitin. "Palladium-Catalysed Coupling Reactions En Route to Molecular Machines: Sterically Hindered Indenyl and Ferrocenyl Anthracenes and Triptycenes, and Biindenyls." Molecules 25, no. 8 (2020): 1950. http://dx.doi.org/10.3390/molecules25081950.

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Pd-catalysed Stille and Suzuki cross-couplings were used to prepare 9-(3-indenyl)-, 6, and 9-(2-indenyl)-anthracene, 7; addition of benzyne led to the 9-Indenyl-triptycenes, 8 and 9. In 6, [4 + 2] addition also occurred to the indenyl substituent. Reaction of 6 through 9 with Cr(CO)6 or Re2(CO)10 gave their M(CO)3 derivatives, where the Cr or Re was complexed to a six- or five-membered ring, respectively. In the 9-(2-indenyl)triptycene complexes, slowed rotation of the paddlewheel on the NMR time-scale was apparent in the η5-Re(CO)3 case and, when the η6-Cr(CO)3 was deprotonated, the resulting
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13

Duarte, Mônica Oliveira, Soraia Lunardelli, Cíntia Janine Kiekow, et al. "Phloroglucinol Derivatives Present an Antidepressant-like Effect in the Mice Tail Suspension Test (TST)." Natural Product Communications 9, no. 5 (2014): 1934578X1400900. http://dx.doi.org/10.1177/1934578x1400900522.

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The antidepressant-like effects of phloroglucinol and seven synthetic related derivatives were investigated using the tail suspension test (TST) in mice. Compounds 2-methyl-1-[2,4,6-trihydroxy-3-(2-methylpropanoyl)phenyl] propan-1-one (5), 1-(2,4,6-trihydroxyphenyl)ethan-1-one (6), 1-(3-acetyl-2,4,6-trihydroxyphenyl)ethan-1-one (7), 2-methyl-1-[2,4,6-trihydroxy-3-(2-methylpropanoyl)-5-{[2,4,6-trihydroxy-3,5-bis(2-methylpropanoyl)phenyl]methyl} phenyl] propan-1-one (9) and 1-{3-acetyl-5-[(3,5-diacetyl-2,4,6-trihydroxyphenyl)methyl]-2,4,6-trihydroxyphenyl}ethan-1-one (10), containing acyl groups
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14

Heuer, Lutz, Ulrike K. Bode, Peter G. Jones, and Reinhard Schmutzler. "Cyclopentadienyldifluorphosphin und Homologe als Liganden in cis-Dichloroplatin(II)-Komplexen — Struktur von cis-(C5Me5PF2)2PtCl2 und cis-(C9H7PF2)[(C9H7)3P]PtCl2 (C5Me5 = Pentamethylcyclopentadienyl, C9H7 = Indenyl) / Cyclopentadienyldifluorophosphine and its Homologues as Ligands in cis-Dichloroplatinum(II) Complexes — Structure of cis-(C5Me5PF2)2PtCl2 and cis-(C9H7PF2)[(C9H7)3P]PtCl2 (C5Me5 = Pentamethylcyclopentadienyl, C9H7 = Indenyl)." Zeitschrift für Naturforschung B 44, no. 9 (1989): 1082–92. http://dx.doi.org/10.1515/znb-1989-0915.

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Derivatives of cyclopentadienyldifluorophosphine. e. g. CpPF2 (1), Cp*PF2 (Cp* = C5Me5) (2),1-(indenyl)PF2 (3), 9-(fluorenyl)PF2 (4), 1-(ferrocenyl)PF2 (5), 1,1′-(ferrocenyl)(PF2)2 (6) and also 1-N-phenyl-2-difluorophosphinopyrrole (7) were prepared using the reaction of the appropriate organolithium compound and PF2Cl. Their reactivity towards cis-dichloro-(η4-cyclooctadiene)-platinum(II) and tetracyanoethylene was investigated. The complexes poly-dichloro-bis-(cyclopentadienyldifluorophosphine)platinum(II) (8), cis-dichloro-bis-(pentamethylcyclopentadienyldifluorophosphine)platinum(II) (9),
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15

Lamač, Martin, Ivana Císařová, and Petr Štěpnička. "Stereoselective Methylation of 1-(Diphenylphosphanyl)-2-[(methoxycarbonyl)methyl]ferrocene. The Crystal Structures of the Methylated Ester and Its Palladium(II) Complex with an Auxiliary 2-[(Dimethylamino)methyl]phenyl Ligand." Collection of Czechoslovak Chemical Communications 72, no. 8 (2007): 985–95. http://dx.doi.org/10.1135/cccc20070985.

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Treatment of racemic 1-(diphenylphosphanyl)-2-[(methoxycarbonyl)methyl]ferrocene successively with NaN(SiMe3)2 and methyl iodide affords the C-alkylated product, 1-(diphenylphosphanyl)-2-[1-(methoxycarbonyl)ethyl]ferrocene (6), as a mixture of diastereoisomers in ca. 10:1 ratio, from which the major (S,Rp/R,Sp)-diastereoisomer is easily isolated by crystallisation. (S,Rp/R,Sp)-6 reacts with [Pd(LNC)(MeCN)2]ClO4 (LNC = 2-[(dimethylamino-κN)- methyl]phenyl-κC1) to give the cationic bis-chelate complex (S,Rp/R,Sp)-[Pd(LNC)(6-κ2O,P)]- ClO4 (9). The structures of (S,Rp/R,Sp)-6 and 9 have been deter
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16

Gross, Thoralf, Helmut Reinke, and Hartmut Oehme. "Geminal bis(hypersilyl) compounds — the synthesis and structure of bis[tris(trimethylsilyl)silyl]silanes." Canadian Journal of Chemistry 78, no. 11 (2000): 1399–404. http://dx.doi.org/10.1139/v00-136.

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Protodesilylation of diphenylsilane with trifluoromethanesulfonic acid and subsequent reaction of the obtained bis(trifluoromethanesulfonyloxy)silane with tris(trimethylsilyl)silyllithium (1) (molar ratio 1:2) afforded bis[tris(trimethylsilyl)silyl]silane (8). Methyl-bis[tris(trimethylsilyl)silyl]silane (3) and phenyl-bis[tris(trimethylsilyl)silyl]silane (10) were obtained by coupling reactions of 1 with MeHSiCl2 or PhHSiCl2, respectively, (2:1). By treatment with HCBr3, the H-silanes 3, 8, and10 were converted into the bromosilanes [(Me3Si)3Si]2SiR1R2 (9: R1 = R2 = Br; 11: R1 = Me, R2 = Br; 1
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17

Son, Kyung-sun, Jeong Oh Woo, Daeyoung Kim, and Sung Kwon Kang. "Crystal structure of dichlorido{2,6-bis[(3-phenyl-1H-pyrazol-1-yl)methyl]pyridine}cobalt(II)." Acta Crystallographica Section E Crystallographic Communications 71, no. 4 (2015): m75—m76. http://dx.doi.org/10.1107/s2056989015003862.

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In the title complex, [CoCl2(C25H21N5)], the CoIIatom is coordinated by two Cl atoms and two N atoms, provided by a tridentate pyrazolylpyridyl ligand, forming a slightly distorted tetrahedral geometry [range of angles: 96.51 (10) (chelate ring) to 118.60 (9)°]. The dihedral angle between Cl/Co/Cl and N/Co/N planes is 86.83 (7)°. The chelate ring has the conformation of a distorted boat. The dihedral angle between pyridyl ring and the coordinated pyrazolyl ring is 56.16 (12)°. The uncoordinated pyrazolyl ring is almost perpendicular to the pyridyl ring with the dihedral angle of 87.49 (10)°. I
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18

Wang, Boyang, та Jian Wang. "Crystal structure of poly[bis(μ2-bis(4-(1H-imidazol-1-yl)phenyl)amine-κ2N:N′)-bis(nitrato-κO)cadmium(II)], C36H30CdN12O6". Zeitschrift für Kristallographie - New Crystal Structures 234, № 5 (2019): 927–28. http://dx.doi.org/10.1515/ncrs-2019-0150.

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19

Ghani, Nurunajah Ab, Nor Hadiani Ismail, Yoshiaki Noma, and Yoshinori Asakawa. "Microbial Transformation of Some Natural and Synthetic Aromatic Compounds by Fungi: Aspergillus and Neurospora Strains." Natural Product Communications 12, no. 8 (2017): 1934578X1701200. http://dx.doi.org/10.1177/1934578x1701200822.

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Microbial transformation of chalcone (1), 4-hydroxychalcone (2) and 4′-hydroxychalcone (3), 1,1-diphenylmethane (4), 1,3-diphenylacetone (5), 1,3-diphenylpropane (6), bibenzyl (7), ( E)-stilbene (8a)- and ( Z)-stilbenes (8b), and phenylcyclohexane (9), (1 R,2 S)-1-phenyl-2-hydroxycyclohexane (9a) and (1 S,2 R)-1-phenyl-2-hydroxycyclohexane (9b), and a naturally occurring bis-bibenzyl, marchantin A (10) were performed by using Aspergillus niger TBUYN-2 and the other Aspergillus strains, and Neurospora crassa which were capable to hydrogenation and epoxidation of a conjugated double bond, and di
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20

Park, Jinho, Beomsu Jang, Yu Ji Moon, Hakjun Lee, Young Kwan Kim, and Seung Soo Yoon. "Deep Blue Organic Light-Emitting Diodes Based on [7,7-Dimethyl-9-(10-phenylanthracen-9-yl)-7H-Indeno[1,2-f] Isoquinoline] Derivatives." Journal of Nanoscience and Nanotechnology 20, no. 11 (2020): 6648–52. http://dx.doi.org/10.1166/jnn.2020.18759.

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In this study, we synthesized and characterized two novel deep blue emitting materials based on indenoquinoline-substituted phenylanthracene derivatives. Multilayer organic light-emitting diodes were fabricated with the following sequence: indium-tin-oxide (ITO)/4,4′,4″-tris[2-naphthyl(phenyl)amino (2-TNATA)/4,4′-bis(N-N-naphthyl)-N-phenylamino) biphenyl (NPB)/Blue emitting material (1 or 2)/Bathophenanthroline (Bphen)/lithium quinolate (Liq)/Al. A device B using ‘7,7-dimethyl-9-(10-phenylanthracen-9-yl)-7H-indeno[1,2-f] isoquinoline (2)’ as an emitter showed the efficient emission with the lu
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21

Deacon, GB, MJ Oconnor, and GN Stretton. "Organomercury Compounds .XXVIII. The Synthesis and 199Hg N.M.R-Spectra of Some Unsymmetrically Dimercurated Arenes." Australian Journal of Chemistry 39, no. 7 (1986): 953. http://dx.doi.org/10.1071/ch9860953.

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Mercuration of 1-methoxy-2-nitrobenzene (1) with mercuric trifluoroacetate (mole ratio 1 : 1) in trifluoroacetic acid yields 1- methoxy-2-nitro-4-(trifluoroacetatomercurio)benzene (2). With a 1 : 2 mole ratio, (2) and 1-methoxy-2-nitro-4,6- bis(trifluoroacetatomercurio)benzene (3) are obtained, and, with a 1:4 ratio, (3) and a little 1-methoxy-2-nitro-3,4- bis(trifluoroacetatomercurio)benzene (4). are obtained. 2-Nitrophenol (5) with mercuric trifluoroacetate (mole ratio 1 : 2) gives 2-nitro- 4,6-bis(trifluoroacetatomercurio)phenol (6), and vanillin (7) yields 5,6-bis(trifluoroacetatomercurio)
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22

Thokchom, Herojit S., Anita D. Nongmeikapam, and Warjeet S. Laitonjam. "Synthesis of fused pyrazolo-, isoxazolo-, pyrimido-, and pyridopyrimidines." Canadian Journal of Chemistry 83, no. 8 (2005): 1056–62. http://dx.doi.org/10.1139/v05-054.

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A systematic study of the synthesis of the 5,7-diaryl-4-oxo-pyrazolo[3,4-d]pyrimidin-6-thiones (3), 2-phenyl-5,7-bis(2′-methylphenyl)-4-oxo-pyrazolo[3,4-d]pyrimidin-6-thiones (4b), 2(3H)-3-phenyl-5,7-diaryl-4-oxo-pyrazolo[3,4-d]pyrimidin-6-thiones (5), 5,7-diaryl-4-oxo-isoxazolo[5,4-d]pyrimidin-6-thiones (7), 3,5,7-triaryl-2,3-dihydro-4-oxo-isoxazalo[5,4-d]pyrimidin-6-thiones (8), 2-amino-6,8-diaryl-5-oxo-pyrimido[4,5-d]pyrimidin-7-thiones (9), 3,4-dihydro-2-amino-4-phenyl-6,8-diaryl-5-oxo-pyrimido[4,5-d]pyrimidin-7-thiones (10), 3-cyano-6,8-diaryl-2,5-dioxo-pyrido[2,3-d]pyrimidin-7-thiones (1
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23

Siddiqui, Bina Shaheen, Munawwer Rasheed, Firdous Ilyas, Tahsin Gulzar, Rajput Mohammad Tariq, and Syed Naim-ul-Hassan Naqvi. "Analysis of Insecticidal Azadirachta indica A. Juss. Fractions." Zeitschrift für Naturforschung C 59, no. 1-2 (2004): 104–12. http://dx.doi.org/10.1515/znc-2004-1-221.

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As a result of chemical investigation on the ethanolic extract of fresh fruit coatings of Azadirachta indica A. Juss. (neem), twenty-seven compounds were identified in non-polar to less polar fractions which showed pesticidal activity determined by WHO method against Anopheles stephensi Liston. These identifications were basically made through GC-EIMS and were further supported by other spectroscopic techniques, including 13C NMR, UV and FTIR as well as retention indices. Thus sixteen n-alkanes, 1-16; three aromatics 2,6-bis-(1,1- dimethylethyl)-4-methyl phenol (17), 2-(phenylmethylene)-octana
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24

Mao, Meng-Xi, Fang-Ling Li, Yan Shen, et al. "Simple Synthesis of Red Iridium(III) Complexes with Sulfur-Contained Four-Membered Ancillary Ligands for OLEDs." Molecules 26, no. 9 (2021): 2599. http://dx.doi.org/10.3390/molecules26092599.

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Phosphorescent iridium(III) complexes have been widely researched for the fabrication of efficient organic light-emitting diodes (OLEDs). In this work, three red Ir(III) complexes named Ir-1, Ir-2, and Ir-3, with Ir-S-C-S four-membered framework rings, were synthesized efficiently at room temperature within 5 min using sulfur-containing ancillary ligands with electron-donating groups of 9,10-dihydro-9,9-dimethylacridine, phenoxazine, and phenothiazine, respectively. Due to the same main ligand of 4-(4-(trifluoromethyl)phenyl)quinazoline, all Ir(III) complexes showed similar photoluminescence e
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25

Arnold, Donald R., Brian J. Fahie, Laurie J. Lamont, Jacek Wierzchowski, and Kent M. Young. "1,n-Radical ions. The photosensitized (electron transfer) formation of 1,5-radical cations." Canadian Journal of Chemistry 65, no. 12 (1987): 2734–43. http://dx.doi.org/10.1139/v87-455.

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The photosensitized (electron transfer) reactions of 3-phenyl-2,3-dihydrobenzofuran (8a), 5-methyl-3-phenyl-2,3-dihydrobenzofuran (8b), cis and trans-2-methoxy-1-phenylindane (9, cis and trans), 3,3-diphenyltetrahydrofuran (10), and 2,2-diphenyl-1-methoxycyclopentane (11) have been studied using 1,4-dicyanobenzene as an electron-accepting photosensitizer and acetonitrile–methanol (3:1) as solvent. These reaction conditions cause carbon–carbon bond cleavage of analogous acyclic β,β-diphenylethyl ethers to give products derived from the diphenylmethyl radical and the α-oxycarbocation intermediat
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26

Feklicheva (Okul), Ekaterina M., Victor B. Rybakov, Evgeny V. Babaev, and Evgeny N. Ofitserov. "Synthesis and X-ray diffraction of derivatives 2,4-dimethyl-6-oxo-1,6-dihydropyridin-3-carboxamide." Butlerov Communications 60, no. 10 (2019): 1–23. http://dx.doi.org/10.37952/roi-jbc-01/19-60-10-1.

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Based on the synthesized starting 2,4-dimethyl-6-oxo-1,6-dihydropyridin-3-carboxamide crystallizing as a dihydrate, 9 derivatives of it including O- and N-phenacyl substituted products were obtained through original rearrangements and cyclizations. The corresponding oxazolopyridinium perchlorate was obtained from the latter preparation in the presence of acid, from which indolysin was obtained under the action of a nitrogenous base. The obtained molecular and crystal structures of all the compounds were studied by single crystal diffraction: 2,4-dimethyl-6-oxo-1,6-dihydropyridine-3-carboxamide
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27

Wang, Bilin, Jing Shi, Yan Jun Hou, Wen Yi Chu та Zhi Zhong Sun. "The crystal structure of tris(μ2-1,3-bis(4,4,4-Trifluoro-3-oxido-1-(oxo)but-2-en-1-yl)phenyl-/κ4O,O′:O′′,O′′′)-bis(1,2-dimethoxyethane-O,O′)-diterbium(III)". Zeitschrift für Kristallographie - New Crystal Structures 230, № 4 (2015): 371–73. http://dx.doi.org/10.1515/ncrs-2015-0035.

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AbstractC50H38F18O16Tb2, monoclinic, C2/c (No. 15), a = 15.6505(13) Å, b = 12.8157(10) Å, c = 29.4494(24) Å, α = 90.0(0)°, β = 91.9581(9)°, γ = 90.0(0)°, V = 91.9581(9) Å3, Z = 4, Rgt(F) = 0.0262, wRref(F2) = 0.0612, T = 293 K.
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28

Woo, Jeongkyu, Soo Kyung Kang, Ju Hee Han, et al. "Red Phosphorescent Platinum(II) Complexes with Tetradentate Pyridine-Containing Ligands for Organic Light Emitting Diodes." Journal of Nanoscience and Nanotechnology 20, no. 11 (2020): 6669–74. http://dx.doi.org/10.1166/jnn.2020.18758.

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Here, red phosphorescent platinum(II) complexes based on tetradentate pyridine-containing lig-ands are studied. To investigate their electroluminescent properties, multilayer devices were fabricated in the following sequence; ITO (180 nm)/4,4′,4″-Tris[2-naphthyl(phenyl)amino]triphenylamine (2-TNATA) (30 nm)/N, N′-di(1-naphthyl)-N,N′-diphenyl-1,1′-biphenyl)4,4′-diamine (NPB) (20 nm)/ Tris(4-carbazoyl-9-ylphenyl)amine (TCTA) (10 nm)/4,4′-Bis(N-carbazolyl)-1,1′-biphenyl (CBP) (20 nm)/Platinum(II) complex (20 nm)/1,3,5-Tris(1-Phenyl-1H-benzimidazol-2-yl)benzene) (TPBi) (40 nm)/Liq (2 nm)/Al (100 n
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29

Kang, Soo Kyung, Jeongkyu Woo, Ju Hee Han, et al. "Platinum (II) Complexes Based on Tetradentate Pyridine-Containing Ligands for Phosphorescent Organic Light-Emitting Diodes." Journal of Nanoscience and Nanotechnology 20, no. 11 (2020): 6683–87. http://dx.doi.org/10.1166/jnn.2020.18774.

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In this study, we designed and synthesized two phosphorescent emitting materials based on tetradentate pyridine-containing ligands. Their photophysical properties were examined for OLEDs and multilayer devices using these materials were fabricated in the following sequence; ITO (180 nm)/4,4′,4″-Tris[2-naphthyl(phenyl)amino]triphenylamine (2-TNATA) (30 nm)/N,N′-di(1-naphthyl)-N,N′-diphenyl-1,1′-biphenyl)4,4′-diamine (NPB) (20 nm)/Tris(4-carbazoyl-9-ylphenyl)amine (TCTA) (10 nm)/4,4′-Bis(N-carbazolyl)-1,1′-biphenyl(CBP): 5, 8, 15% Platinum (II) complexes (20 nm)/1,3,5-Tris(1-Phenyl-1H-benzimidaz
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Cho, Ching-Sheng, Wen-Bin Liau, and Leo-Wang Chen. "Single-crystal structure analysis of a novel aryl phosphinate diglycidyl ether." Acta Crystallographica Section B Structural Science 55, no. 4 (1999): 525–29. http://dx.doi.org/10.1107/s010876819900018x.

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The crystal structure of 10-[2,5-bis(2,3-epoxy-1-propoxy)phenyl]-9-oxa-10-phosphaphenanthren-10-one has been studied by single-crystal X-ray diffraction. The unit cell of C24H21O6P, M r = 436.4, is triclinic, P1¯, with a = 8.507 (3), b = 10.613 (4), c = 12.457 (3) Å, α = 80.05 (3), β = 71.38 (2), γ = 76.69 (3)°, V = 1031.1 (6) Å3, Z = 2, D x = 1.406 Mg m−3 and μ(Mo Kα) = 0.17 mm−1. The final R (wR) is 0.063 (0.057) {w = 1/[σ2(F) + 0.0004F 2]} for 3619 unique reflections measured at 295 K. The aryl phosphinate group bonded to the central phenyl ring comes close to one of the two glycidyl ether
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31

Soman, Anjaly, and K. N. Narayanan Unni. "Enhancement in electron transport and exciton confinement in OLEDs: role of n-type doping and electron blocking layers." European Physical Journal Applied Physics 86, no. 1 (2019): 10201. http://dx.doi.org/10.1051/epjap/2019190020.

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Doped transport layers are essential for achieving high efficiency in organic light emitting diodes (OLEDs). We have studied the effect of doping the electron transport layer (ETL), tris-(8-hydroxyquinoline) aluminum (Alq3) with different percentages of lithium fluoride (LiF). We have also studied the effect of different electron blocking layers (EBLs) such as Tris (4-carbazoyl-9-ylphenyl)amine (TCTA), N,N'-Bis (naphthalen-1-yl)-N,N'-bis(phenyl)-benzidine(NPB), and Di-[4-(N,N-di-p-tolyl-amino)-phenyl]cyclohexane (TAPC) in an Alq3:2,3,6,7-Tetrahydro-1,1,7,7,-tetramethyl-1H, 5H, 11H −10-(2-benzo
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32

Beckmann, Jens, Jens Bolsinger, and Andrew Duthie. "The Reactivity of Diorganotellurium Oxides Towards Phenol and o-Nitrophenol. Hypervalent and Secondary Bonding of Four Different Product Classes." Australian Journal of Chemistry 61, no. 3 (2008): 172. http://dx.doi.org/10.1071/ch07329.

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The reaction of the diorganotellurium oxides R2TeO (R = Ph, p-MeOC6H4, p-Me2NC6H4) with phenol and o-nitrophenol produces diorganotellurium hydroxy phenolates, R2Te(OH)OPh (1, R = Ph; 2, R = p-MeOC6H4; 3, R = p-Me2NC6H4), diorganotellurium bis(phenolates) R2Te(OPh)2 (4, R = Ph; 5, R = p-MeOC6H4; 6, R = p-Me2NC6H4), tetraorganoditelluroxane bis(o-nitrophenolates), (R′O)R2TeOTeR2(OR′) (7, R = p-MeOC6H4; 8, R = p-Me2NC6H4; R′ = o-NO2C6H4), and a hexaphenyltritelluroxane bis(o-nitrophenolate) (R′O)Ph2TeOTePh2OTePh2(OR′) (9, R′ = o-NO2C6H4), respectively. The redistribution reactions of R2Te(OPh)2
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33

Amr, Abdel-Galil E. "Synthesis of Some New Linear and Chiral Macrocyclic Pyridine Carbazides as Analgesic and Anticonvulsant Agents." Zeitschrift für Naturforschung B 60, no. 9 (2005): 990–98. http://dx.doi.org/10.1515/znb-2005-0914.

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A series of 2,6-disubstituted pyridine derivatives were prepared from 2,6-diacetylpyridine or 2,6- dicarbonyl pyridine dichloride as starting materials. Reaction of 2,6-diacetylpyridine 1 with hydroxylamine hydrochloride or different aromatic aldehydes afforded the corresponding 2,6-diacetylpyridine dioxime and 2,6-bis-[β -(2-thienyl)acryloyl]pyridine derivatives 2 and 3, respectively. Additionally, N2,N2‘-(pyridine-2,6-dicarbonyl)-L-amino acid hydrazides 5 were prepared starting from 2,6- dicarbonyl pyridine dichloride via the corresponding esters 4. Compound 3 was reacted with hydroxylamine
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34

Hintermaier, Frank, Sylvia Helding, Leonid B. Volodarsky, Karlheinz Sünkel, Kurt Polbom та Wolfgang Beck. "Übergangsmetallkomplexe mit Nitroxidradikalen: Palladium-, Platin-, Pentamethylcyclopentadienyl-rhodium- und -iridium-Komplexe sowie α-Aminocarboxylatkomplexe mit Donor-haltigen Derivaten des 2,5-Dihydroimidazol-l-oxyls / Transition Metal Complexes of Nitroxide Radicals, Palladium, Platinum, Pentamethylcyclopentadienyl Rhodium and Iridium Complexes, and α-Aminocarboxylate Complexes with Derivatives of 2,5-Dihydroimidazole-l-oxyls". Zeitschrift für Naturforschung B 53, № 1 (1998): 101–9. http://dx.doi.org/10.1515/znb-1998-0118.

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2,5-Dihydroimidazoline-l-oxyl radicals I, II with imino substituents coordinate to Pd(II) and Pt(II) complexes with formation of the N,N chelate complexes 1-6. With oxygen containing substituents either monodentate N-coordination to give 8 or N ,O chelate formation to give 9 takes place, depending on the position of the oxygen atom relative to the ring nitrogen atom. With radicals III that also have the second ring nitrogen atom oxidized and the Rh(III) or Ir(III) complexes [Cp*MCl2]2 the O , O chelates 11 -13 could be obtained, while with Na2PdCl4 the heterocycle was destroyed with formation
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35

Robertson, Katherine N., Pradip K. Bakshi, Susanne D. Lantos, T. Stanley Cameron, and Osvald Knop. "Crystal chemistry of tetraradial species. Part 9. The versatile BPh4- anion, or how organoammonium H(N) atoms compete for hydrogen bonding." Canadian Journal of Chemistry 76, no. 5 (1998): 583–611. http://dx.doi.org/10.1139/v98-077.

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In organoammonium cations containing two or more N atoms, the H(N) atom introduced by the protonation may engage in an N→H(N)...Y bond to an external acceptor (anion or solvent molecule); in an intra-cation (intra-annular) N→H(N)...N' bond; or in a branched N→H(N)...N',Y bond(s), simultaneously intra-cation and to one or more external acceptors. The outcome of the competition for these bond types is determined by various factors, e.g., the size of the ring to be closed by insertion of the H(N) atom, steric accessibility of H(N), and the H-bond-forming strength of Y. Some of these are discussed
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36

Farkens, Michael, Thomas G. Meyer, Ion Neda та ін. "Zur Chemie der l,3,5-Triaza-2-phosphinan-4,6-dione. Teil VI. Darstellung von 1,3,5-Triaza-2 λ3-, 1,3,5-Triaza-2 λ4- und 1,3,5-Triaza-2 λ5-phosphinan-4,6-dionen / Chemistry of the 1,3,5-Triaza-2-phosphinane-4,6-diones. Part VI. Synthesis of 1,3,5-Triaza-2λ3-, 1,3,5-Triaza-2λ4- and 1,3,5-Triaza-2λ5-phosphinane-4,6-diones". Zeitschrift für Naturforschung B 49, № 2 (1994): 145–64. http://dx.doi.org/10.1515/znb-1994-0201.

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The reactions of 1,3,5-trimethylbiuret with dicyclohexylaminodichlorophosphine and with pyrrolidinodichlorophosphine furnished the triazaphosphinane-diones 1 and 2. Oxidation reactions of the 2-diorganoam ino-1,3,5-triorgano-1,3,5-triaza-2 λ3-phosphinane-4,6-diones 1, 2, and 4-9, as well as 2-fluoro-1,3,5-trimethyl-1,3,5-triaza-2λ3-phosphinane-4,6-dione 10 with hydrogen peroxide, elemental sulphur, phenyl azide, 1-adamantyl azide,p-nitrobenzoyl azide, tetrachloro-orthobenzoquinone, tetrabromo-orthobenzoquinone, 3,5-di-t-butyl-orthobenzoquinone, and hexafluoroacetone led to the respective oxida
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37

Klein, Hans-Friedrich, Xiaoyan Li, Ulrich Flörke, and Hans-Jürgen Haupt. "Hydrido(acylenolato)cobalt(III)-Verbindungen mit Trimethylphosphan- Liganden: Insertionsreaktionen mit Alkinen und die ersten Carbonylcobalt(III)-Komplexe / Hydrido(acylenolato)cobalt(III) Compounds Containing Trimethylphosphane Ligands: Insertion Reactions with Alkynes and the First Carbonylcobalt(III) Complexes." Zeitschrift für Naturforschung B 55, no. 8 (2000): 707–17. http://dx.doi.org/10.1515/znb-2000-0807.

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Abstract Formal insertion of phenylethyne into Co-H functions of mer-octahedral acyl(enolato)-cobalt(III) hydrides 1-3 proceeds under ambient conditions affording η1-vinylcobalt(III) compounds where the dianionic acyl(enolato) ligands are derived from 2-formyl-4-phenyl-cyclohexanone (4), 1-formyl-cyclohexan-2-one (5), and 3-hydroxo-2,3-diphenyl-propenal (6). Dissociation and association of trimethylphosphane results in a reversible transformation of penta-coordinate complexes 4 -6 into hexa-coordinate ones 7 -9, respectively, involving different tautomeric vinyl species. In toluene solution 9
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38

Loh, Claas, Carsten Glock, Steffen Ziemann, Helmar Görls, Sven Krieck, and Matthias Westerhausen. "Synthesis and Characterization of Strontium Bis(N-isopropylanilide) and Comparison with the Lighter Magnesium and Calcium Congeners." Zeitschrift für Naturforschung B 68, no. 5-6 (2013): 518–32. http://dx.doi.org/10.5560/znb.2013-3044.

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The metathesis reaction of strontium diiodide [(thf)5SrI2] with K[N(Ph)iPr] in THF yields [(thf)4Sr{N(Ph)iPr}2] (1). Ligand exchange reactions with 1,2-dimethoxyethane (DME), tetramethylethylenediamine (TMEDA), and pentamethyldiethylenetriamine (PMDETA) allow the isolation of the corresponding adducts [(dme)2Sr{N(Ph)iPr}2] (2), [(tmeda)(thf)Sr{N(Ph)iPr}2] (3) and [(pmdeta)Sr{N(Ph)iPr}2] (4), respectively. Magnesiation of N-isopropylaniline with dibutylmagnesium in THF leads to the formation of [(thf)2Mg{N(Ph)iPr}2] (5). A similar reaction in TMEDA gives nearly insoluble crystalline [(tmeda)Mg{
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39

Koradecka, Danuta, and Jolanta Skowroń. "The activity of the Interdepartmental Commission for Maximum Admissible Concentrations and Intensities for Agents Harmful to Health in the Working Environment in 2017 and the work plan in 2018." Podstawy i Metody Oceny Środowiska Pracy 34, no. 1(95) (2018): 111–29. http://dx.doi.org/10.5604/01.3001.0011.5835.

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In 2017, the Commission met at three sessions, in which 16 documentations for recommended exposure limits of chemical substances were discussed. Moreover, the Commission discussed: − the positions of the Interdepartmental Commission for MAC and MAI regarding: smog, limit value of nitric oxide in the underground mining and tunnels sector and binding value for 1,2-dichloroethane − introduction of the "skin" notation (substances absorption through the skin may be important as in the case of inhalation) for chemical substances included in the regulation of the Minister of Labour and Social Policy
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40

Ibraheam, Israa Adnan, Imad Hadi Hameed S., and Haider Mashkoor Hussein. "Cyclamen persicum: Methanolic Extract Using Gas Chromatography-Mass Spectrometry (GC-MS) Technique." International Journal of Pharmaceutical Quality Assurance 8, no. 04 (2017). http://dx.doi.org/10.25258/ijpqa.v8i04.10546.

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Cyclamen was traditionally classified in the family Primulaceae, was reclassified in the subfamily Myrsinoideae within the family Primulaceae. The objective of this study was analysis of the secondary metabolite products. Bioactives are chemical compounds often referred to as secondary metabolites. Thirty eight bioactive compounds were identified in the methanolic extract of Cyclamen persicum. The identification of bioactive chemical compounds is based on the peak area, retention time molecular weight and molecular formula. GC-MS analysis of Cyclamen persicum revealed the existence of the3-Oxo
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Percino, M., Maria Castro, Margarita Ceron, Guillermo Soriano-Moro, Victor Chapela, and Francisco Melendez. "X-ray molecular structure and theoretical study of 1,4-bis[2-cyano-2-(o-pyridyl)ethenyl]benzene." Chemical Papers 68, no. 2 (2014). http://dx.doi.org/10.2478/s11696-013-0434-5.

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AbstractThe structural characterisation of the molecule 1,4-bis[2-cyano-2-(o-pyridyl)ethenyl] benzene obtained through Knoevenagel condensation is reported. The single crystals, as light brown rods, were cultured from a chloroform solution using a slow evaporation method at ambient temperature. The compound crystallised in the monoclinic system belonging to the C2/c space group with a = 26.4556(9) Å, b = 3.73562(10) Å, c = 18.4230(6) Å, β = 109.841(4)° and the asymmetric unit comprising Z = 4. The structure is ordered and the molecules of the title compound exhibited a lattice with water molec
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