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Journal articles on the topic '3-propanedione'

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1

Aakeröy, Christer B., Izhar Hussain, Safiyyah Forbes, and John Desper. "Versatile Ligands for the Construction of Layered Metal-Containing Networks." Australian Journal of Chemistry 62, no. 8 (2009): 899. http://dx.doi.org/10.1071/ch08440.

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The synthetic opportunities furnished by organic synthesis and the inherent structure-directing possibilities of coordination complexes have been combined in the assembly of a series of layered metal-containing hybrid materials. The supramolecular assembly relies on self-complementary non-covalent interactions, and in five of the six structures presented herein, N–H···O=C hydrogen bonds between acetamide moieties on neighbouring ligands provide the primary structure-direction tool as intended. The distances between metal ions are controlled by ligand···ligand hydrogen bonds and reside within a
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2

Brown, Joshua J., Aidan J. Brock, Michael C. Pfrunder, et al. "Co-Crystallisation of 1,4-Diiodotetrafluorobenzene with Three Different Symmetric Dipyridylacetylacetone Isomers Produces Four Halogen-Bonded Architectures." Australian Journal of Chemistry 70, no. 5 (2017): 594. http://dx.doi.org/10.1071/ch16673.

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The co-crystallisation behaviour of three symmetrical dipyridylacetylacetone ligands (1,3-di(2-pyridyl)-1,3-propanedione (o-bppdH), 1,3-di(3-pyridyl)-1,3-propanedione (m-bppdH), and 1,3-di(4-pyridyl)-1,3-propanedione (p-bppdH)), with the linear halogen-bond donor 1,4-diiodotetrafluorobenzene (1,4-DITFB) has been investigated. The reaction of these components under ambient conditions in a 1 : 1 stoichiometry produced four halogen-bonded assemblies ([o-bppdH·1,4-DITFB, [m-bppdH·1,4-DITFB], [2(m-bppdH)·1,4-DITFB], and [p-bppdH·1,4-DITFB]). The combination of multiple supramolecular interactions i
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3

P., VENUGOPALAN, and KRISHNANKUTTY K. "Binuclear Metal Chelates of 1-(2-Hydroxyphenyl)-3-phenyl-1 ,3-propanedione." Journal of Indian Chemical Society Vol. 74, Jul 1997 (1997): 564–65. https://doi.org/10.5281/zenodo.5908743.

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Department of Chemistry. University of Calicut, Kerala-673 635 <em>Manuscript received 29 December 1995, accepted 14 May 1996</em> Binuclear Metal Chelates of 1-(2-Hydroxyphenyl)-3-phenyl-1 ,3-propanedione.
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4

Wallet, J. C., E. Molins, and C. Miravitlles. "1-Phenyl-3-(3,4,5-trimethoxyphenyl)-1,3-propanedione." Acta Crystallographica Section C Crystal Structure Communications 51, no. 1 (1995): 103–4. http://dx.doi.org/10.1107/s0108270194007687.

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5

Bertolasi, Valerio, Loretta Pretto, Gastone Gilli та Paola Gilli. "π-Bond cooperativity and anticooperativity effects in resonance-assisted hydrogen bonds (RAHBs)". Acta Crystallographica Section B Structural Science 62, № 5 (2006): 850–63. http://dx.doi.org/10.1107/s0108768106020933.

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Bond cooperativity effects, which are typical of `resonant' chains or rings of π-conjugated hydrocarbons, can also occur in hydrogen-bonded systems in the form of σ-bond and π-bond cooperativity or anticooperativity. σ-Bond cooperativity is associated with the long chains of O—H...O bonds in water and alcohols while σ-bond anticooperativity occurs when the cooperative chain is interrupted by a local defect reversing the bond polarity. π-Bond cooperativity is the driving force controlling resonance-assisted hydrogen bonds (RAHBs), while π-bond anticooperativity has never been considered so far
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6

Bermejo, Elena, Alfonso Castiñeiras, and Douglas X. West. "Structural Study of an N(4)-Substituted Thiosemicarbazone Prepared from 1-Phenyl-1,2-propanedione-2-oxime, and of a Related Nickel(II) Complex." Zeitschrift für Naturforschung B 56, no. 4-5 (2001): 369–74. http://dx.doi.org/10.1515/znb-2001-4-508.

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Abstract 1-Phenyl-1,2-propanedione-2-oxime reacts with 3-piperidylthiosemicarbazide and 3-hexamethyleneiminylthiosemicarbazide to give the respective 1-phenyl-1,2-propanedione-1-thiosemicarbazone-2-oximes, HPopip and HPohexim. The crystal structure of HPopip shows the oxime and thiosemicarbazone moieties in a conformation single-trans respect to carbon-carbon. A six-coordinate nickel(II) complex, [Ni(Pohexim)2], has two monoanionic (through loss of a proton from the thiosemicarbazone function) oxime-thiosemicarbazone ligands coordinated in a meridonal arrangement via the oxime nitrogen, the th
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7

Hasan, Najmul, and Khalid Iftikhar. "Syntheses, crystal structure and photophysical properties of [Sm(dbm)3(impy)] and [Tb(dbm)3(impy)] and their hybrid films." New Journal of Chemistry 43, no. 11 (2019): 4391–405. http://dx.doi.org/10.1039/c8nj05045g.

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This paper reports the syntheses, crystal structure and photophysical properties of eight-coordinate complexes [Sm(dbm)<sub>3</sub>(impy)] and [Tb(dbm)<sub>3</sub>(impy)] (dbm is the anion of 1,3-diphenyl-1,3-propanedione and impy is 2-(1H-imidazol-2-yl)pyridine).
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8

Ng, Seik Weng, Abdul Hamid Othman, and Sri Nurestri Abdul Malek. "Crystal structures of 1-(2-hydroxyphenyl)-3-phenyl-1,3-propanedione and 1-(1,3-benzodioxol-5-yl)-3-(2,4-dimethoxyphenyl)-1,3-propanedione." Journal of Chemical Crystallography 24, no. 5 (1994): 331–35. http://dx.doi.org/10.1007/bf01670209.

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9

S.D., Thakur, P. Munot K., D. Deshmukh R., and Tihile M.S. "Studies in influence of ionic strength of medium on the complex equilibria of substituted hydroxy-1,3-popandiones with CIII and LaIII metal ions pH metrically." Journal of Indian Chemical Society Vol. 89, Oct 2012 (2012): 1399–404. https://doi.org/10.5281/zenodo.5771314.

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R.D.I.K. &amp; N.K.D. CoiJege, Badnera (Riy.), Amravati-444 701, Maharashtra, India <em>E-mail</em> : sdthakur1968@indiatimes.com S.P.M. College, Ghatanji, Dist. Yavatmal, Maharashtra, India <em>Manuscript received 26 September 2011, revised 30 January 2012, accepted 31 January 2012</em> The solution studies (the proton-ligand stability constant pK and metal-ligand stability constants log <em>K</em>) of binary (1 : 1) complexes or Cr<sup>Ill</sup> and La<sup>llI</sup>&nbsp;with 1-(2&#39;-hydroxy-S&#39;-bromophenyl)-3-(2&#39;-chlorophenyl)-1,3-propanedione [HB2CP] [L<sub>1</sub>] and 1-(2&#39;-
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10

Gilli, P., V. Ferretti, V. Bertolasi, and G. Gilli. "Structure of 3-(p-chlorophenyl)-1-phenyl-1,3-propanedione enol." Acta Crystallographica Section C Crystal Structure Communications 48, no. 10 (1992): 1798–801. http://dx.doi.org/10.1107/s0108270192001719.

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11

Stomberg, Rolf, Vratislav Langer, and Marcelle Hauteville. "1-(2-Hydroxy-4,6-dimethoxy-3-methylphenyl)-3-(4-methoxyphenyl)-2-methyl-1,3-propanedione." Acta Crystallographica Section E Structure Reports Online 58, no. 10 (2002): o1116—o1118. http://dx.doi.org/10.1107/s1600536802016136.

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12

Castro-Tamay, Pablo, David Villaman, Jean-René Hamon, and Néstor Novoa. "Isolated Dipolar ONN Schiff Base Regioisomers: Synthesis, Characterization and Crystallographic Study." Molecules 29, no. 24 (2024): 5863. https://doi.org/10.3390/molecules29245863.

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Organic compounds with 1,3-diketone or 3-amino enone functional groups are extremely important as they can be converted into a plethora of carbo- or heterocyclic derivatives or can be used as ligands in the formation of metal complexes. Here, we have achieved the preparation of a series of non-symmetrical β-ketoenamines (O,N,N proligand) of the type (4-MeOC6H4)C(=O)CH=C(R)NH(Q) obtained through the Schiff base condensation of 1,3-diketones (1-anisoylacetone, 1-anisyl-3-(4-cyanophenyl)-1,3-propanedione, and 1-anisyl-3-(4,4,4-trifluorotolyl)-1,3-propanedione) functionalized with electron donor a
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13

Casellato, U., R. Graziani, G. Maccarone, R. R. Purello, and M. Vidali. "Crystal structure of 1-(2-hydroxyphenyl)-3-(2-thiomethoxyphenyl)-1,3-propanedione, C16H14O3S." Journal of Crystallographic and Spectroscopic Research 17, no. 3 (1987): 323–29. http://dx.doi.org/10.1007/bf01161431.

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14

Blasi, Delia, Pierluigi Mercandelli та Lucia Carlucci. "Supramolecular Frameworks and a Luminescent Coordination Polymer from New β-Diketone/Tetrazole Ligands". Inorganics 10, № 4 (2022): 55. http://dx.doi.org/10.3390/inorganics10040055.

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Mixed multidentate linkers with donor groups of different types can be fruitfully exploited in the self-assembly of coordination polymers (CPs) and Metal-Organic Frameworks (MOFs). In this work we develop new ligands containing a β-diketone chelating functionality, to better control the stereochemistry at the metal center, and tetrazolyl multidentate bridging groups, a combination not yet explored for networking with metal ions. The new ligands, 1,3-bis(4-(1H-tetrazol-5-yl)phenyl)-1,3-propanedione (H3L1) and 1-phenyl-3-(4-(1H-tetrazol-5-yl)phenyl)-1,3-propanedione (H2L2), are synthesized from
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15

Tejaswini, S.Bante, and M.M.Rathore. "Microwave Assisted Synthesis of some new Chromone and their Antibacterial Activity." International Journal of Trend in Scientific Research and Development 1, no. 5 (2017): 1132–34. https://doi.org/10.31142/ijtsrd2428.

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Chlorosubstitued3 Aroylchromone were prepared by refluxing of 1 2 hydroxy 5 chlorophenyl 3 2&#39; furyl 1,3 propanedione and glutaraldehyde in ethanol and piperidine..The newly synthesized Chlorosubstitued 3 Aroylchromone were characterized on the basis of elemental analysis and spectroscopic data of IR,NMR. The titled compound were evaluated for their antibacterial activity against species such as Escherichia coli, Staphylococcus aureaus, Bacillus subtilis and Pseudomons aeruginosa Tejaswini S.Bante | M.M.Rathore &quot;Microwave Assisted Synthesis of some new Chromone and their Antibacterial
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16

Joglekar, S. J., and S. D. Samant. "Abnormal base catalysed reaction of formaldehyde and benzaldehydes with 1-(2-hydroxyphenyl)-3-phenyl-1, 3-propanedione." Tetrahedron Letters 29, no. 2 (1988): 241–44. http://dx.doi.org/10.1016/s0040-4039(00)80065-9.

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17

Moriguchi, Tetsuji, Kenji Yoza, and Akihiko Tsuge. "Synthesis, Characterization, and Crystal Structure of Pyridinium Tetrakis{1-trifluoromethyl-3-(1′-pyreno)-1,3-propanedionato}lanthanate(III) Complex." Journal of Crystallography 2014 (September 30, 2014): 1–6. http://dx.doi.org/10.1155/2014/271238.

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The reaction of 1-trifluoromethyl-3-(1′-pyreno)-1,3-propanedione with lanthanum(III) trichloride in the presence of pyridine leads to halide ligand exchange, yielding a novel pyridinium tetrakis{1-trifluoromethyl-3-(1′-pyreno)-1,3-propanedionato}lanthanate(III) complex with four polycyclic aromatic hydrocarbon moieties. This reaction easily proceeds under mild conditions (25°C, 24 h) producing the complex in a 90% isolated yield. The complex was characterized by infrared spectroscopy, proton nuclear magnetic resonance spectroscopy, and positive fast atom bombardment mass spectrometry, and its
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18

Li, X., and Y. Q. Zou. "Crystal structure of 1-(2-furyl)-3-(p-methoxyphenyl)-1,3-propanedione, C14H12O4, the enol form." Zeitschrift für Kristallographie - New Crystal Structures 219, no. 1-4 (2004): 301–2. http://dx.doi.org/10.1524/ncrs.2004.219.14.301.

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19

R., N. Prasad, and Sharma Priyanka. "Synthesis and characterization of NiII, CuII and ZnII complexes of 18-membered oxaazamacrocycles." Journal of Indian Chemical Society Vol. 88, May 2011 (2011): 665–72. https://doi.org/10.5281/zenodo.5769043.

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Department of Chemistry, University of Rajasthan, Jaipur-302 055, Rajasthan, India <em>E-mail</em> : rnp 1949@yahoo.co. in <em>Manuscript received 11 January 2010, revised 03 September 2010, accepted 05 October 2010</em> Complexes of the type [MLCI]CI and ZnLCl<sub>2</sub> (where M = Ni<sup>II</sup> and Cu<sup>II</sup> and L= IS-membered macrocycle containing N<sub>2</sub>O<sub>3</sub> donor set) have been synthesized by template condensation of 1,13-diamino-4, 7 ,10-trioxatridecane with &szlig;-diketones such as 2,4- entanedione, 1-phenyl-1,3-butanedione and 1,3-diphenyl-1,3-propanedione. The
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20

N., B. L. Prasad, and Hussain Reddy K. "Spectrophotometric determination of nickel(II) in aqueous medium using 1-phenyl-1,2-propanedione-2-oxime." Journal of India Chemical Society Vol 81, Sep 2004 (2004): 794–96. https://doi.org/10.5281/zenodo.5833294.

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Oil Technological Research Institute, JNTU, Anantapur-5 15 001, India Department of Chemistry, Sri Krishnadevaraya University, Anantapur-5 15 003, India <em>Fax</em>: 91-8554-29043 <em>Manuscript received 11 September 2002, revised 20 October 2003, accepted 6 April 2004</em> The reagent 1-phenyl-1,2-propanedione-2-oxime thiosemicarbazone (PPDOT) gives brownish yellow coloured complex with nickel(II) in sodium acetate-acetic acid buffer solution. The molar absorptivity and Sandell&#39;s sensitivity of Ni<sup>II</sup>-PPDOT complex are 1.2 x 10<sup>4</sup> dm<sup>3</sup> mol<sup>-1</sup> cm<sup>
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21

MAMEDOV, V. A., V. L. POLUSHINA, F. F. MERTSALOVA, I. A. NURETDINOV, and A. KH PLYAMOVATYI. "ChemInform Abstract: Medium Effects on the Reactions of 3-Chloro-1,3-diphenyl-1,2- propanedione with ortho-Phenylenediamine." ChemInform 24, no. 19 (2010): no. http://dx.doi.org/10.1002/chin.199319190.

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22

Mamedov, V. A., V. L. Polushina, F. F. Mertsalova, I. A. Nuretdinov, and A. Kh Plyamovatyi. "Medium effect on the direction of the reaction of 3-chloro-1,3-diphenyl-1,2-propanedione with ortho-phenylenediamine." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 40, no. 7 (1991): 1472–74. http://dx.doi.org/10.1007/bf00961256.

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23

Teixidor, F., T. Flor, and J. Casabo. "Alkaline earth metal complexes with the non-cyclic oxygen-containing ligand: 1,3-Bis(2-hydroxyphenyl)-l,3-propanedione." Inorganica Chimica Acta 118, no. 2 (1986): 125–28. http://dx.doi.org/10.1016/s0020-1693(00)81373-0.

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24

R., N. Prasad, and Sharma Nisha. "Template synthesis of alkaline earth metal complexes of oxa-azamacrocycles derived from P-diketones." Journal of Indian Chemical Society Vol. 89, Jan 2012 (2012): 29–34. https://doi.org/10.5281/zenodo.5751254.

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Department of Chemistry, University of Rajasthan, Jaipur-302 055, Rajasthan, India <em>E-mail</em> : rnp _1949@yahoo.co.in <em>Manuscript received 08 October 2010, revised 07 April 2011, accepted 20 April 2011</em> Complexes of the type<strong> </strong>[MLCl]Cl (where M = Mg<sup>ll</sup>, Ca<sup>ll</sup>, Sr<sup>II</sup> an Ba<sup>II</sup> ; L = N<sub>2</sub>O<sub>3</sub> type macrocycle having IS-membered ring) have been synthesized by 1 + 1 cyclocondensation of l, 13-diamino-4, 7,1 0-trioxatridecane and &beta;-diketones such as 2,4-pentanedione, 1-phenyl-1,3-butanedione or 1,3-diphenyl-1,3-
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25

V. Palermo, D. Ruiz, A. Sathicq, P. Vázquez, and G. Romanelli. "A hybrid system bases on silica-alumina and Keggin heteropolyacids as catalyst in the suitable 2-(2-furyl)-chromones and chromanones synthesis." Ciencia en Desarrollo 13, no. 1 (2022): 93–102. http://dx.doi.org/10.19053/01217488.v13.n1.2022.14165.

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Molybdophosphoric acid/silica-alumina composites are synthesized a through a process described, in which the heteropolyacid was impregnated on different silica-aluminas, obtained by sol-gel. Three different techniques were used to prepare the samples. The catalysts were prepared by incipient wetness impregnation and different thermal treatments were applied. The hybrid systems were characterized by using SBET, DRX, XRD and acidity measurements. The catalytic activity of these materials was tested in the solvent-free cyclization of 1-(2-hydroxyphenyl)-3-(2-furyl)-1,3-propanedione to 2-(2-furyl)
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26

Li, Xiaojing, Lan Yan, Hui Wanyan, and Rudong Yang. "Chelate complexes of 1,3-bis-(1′-phenyl-3′-methyl-5′-pyrazolone-4′)-1,3-propanedione and 1,10-phenanthroline with lanthanide." Polyhedron 12, no. 16 (1993): 2021–25. http://dx.doi.org/10.1016/s0277-5387(00)81476-x.

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27

Ray, Pritha, Jyothi Nagraj, Subhoshree Chatterjee, et al. "A novel series of di-fluorinated propanedione derivatives synergistically augment Paclitaxel mediated caspase 3 activation in ovarian cancer cells." Journal of Cancer Research and Therapeutics 10, no. 3 (2014): 701. http://dx.doi.org/10.4103/0973-1482.138095.

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28

Yohannes, Mulugeta Hailu, Atlabachew Minaleshewa, Singh Chandravanshi Bhagwan, and Redi-Abshiro Mesfin. "Composition of essential oil and antioxidant activity of Khat (Catha edulis Forsk), Ethiopia." Chemistry International 3, no. 1 (2017): 25–31. https://doi.org/10.5281/zenodo.1473050.

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In this study, we determined the chemical composition and antioxidant activities of the essential oils from two different varieties of khat (Catha edulis Forsk) cultivated in Ethiopia. The essential oils were extracted by hydrodistillation using the Clevenger type apparatus, identifications of compounds were made by gas chromatography and gas chromatography-mass spectrometry (GC-MS). Seventy seven different compounds were identified from essential oils of the two different khat cultivars. The essential oils in the samples from Bahir Dar and Wendo were composed of 50 and 34 compounds, respectiv
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Liu, Cai-Ming. "Two Dy2 Zero-Field Single-Molecule Magnets Derived from Hydrazone Schiff Base-Bridging Ligands and 1,3-Di(2-pyridyl)-1,3-propanedione." Magnetochemistry 11, no. 7 (2025): 58. https://doi.org/10.3390/magnetochemistry11070058.

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Two hydrazone Schiff base-bridging ligands with different heterocycles {2-[(E)-(5-chloro-2-hydroxyphenyl)methylidene]diazanyl}(pyrazine-2-yl)methanone (H2LSchiff-1) and (E)-N′-(2-hydroxy-3-methoxybenzylidene)nicotinohydrazide (H2LSchiff-2) together with 1,3-di(2-pyridyl)-1,3-propanedione (Hdpp) were chosen to construct two new Dy2 complexes, [Dy2(LSchiff-1)2(DMF)2(dpp)2]·0.5DMF (1) and [Dy2(LSchiff-2)2(DMF)2(dpp)2]·2DMF (2). Although the [N2O6] coordination spheres are observed for the Dy3+ ions in 1 and 2, their coordination configurations have some differences (both the biaugmented trigonal
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Tsai, Jie-Heng, Li-Sung Hsu, Hsiu-Chen Huang, et al. "1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione Induces G1 Cell Cycle Arrest and Autophagy in HeLa Cervical Cancer Cells." International Journal of Molecular Sciences 17, no. 8 (2016): 1274. http://dx.doi.org/10.3390/ijms17081274.

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Russo, U., M. Vidali, and B. Zarli. "The preparation of the new compartmental ligand 1-(2-hydroxyphenyl)-3-(2-thiomethoxyphenyl)-1,3-propanedione and its interactions with metal ions." Polyhedron 9, no. 22 (1990): 2721–26. http://dx.doi.org/10.1016/s0277-5387(00)86802-3.

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32

Denis, Aline B., Cristina A. Diagone, Ana M. G. Plepis, and Rommel B. Viana. "Kinetic Parameters during Bis-GMA and TEGDMA Monomer Polymerization by ATR-FTIR: The Influence of Photoinitiator and Light Curing Source." Journal of Spectroscopy 2016 (2016): 1–8. http://dx.doi.org/10.1155/2016/6524901.

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This study aimed to analyze the kinetic parameters of two monomers using attenuated total reflectance Fourier transform infrared (ATR-FTIR): 2,2-bis-[4-(2-hydroxy-3-methacryloxypropyl-1-oxy)-phenyl] propane (Bis-GMA) and triethylene glycol dimethacrylate (TEGDMA). The following were calculated to evaluate the kinetic parameters: maximum conversion rate (Rpmax), time at the maximum polymerization rate (tmax), conversion atRpmax, and total conversion recorded at the maximum conversion point after 300 s. Camphorquinone (CQ) and phenyl propanedione (PPD) were used in this study as photoinitiators,
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RUSSO, U., M. VIDALI, and B. ZARLI. "ChemInform Abstract: The Preparation of the New Compartmental Ligand 1-(2-Hydroxyphenyl)-3-( 2-thiomethoxyphenyl)-1,3-propanedione and Its Interactions with Metal Ions." ChemInform 22, no. 13 (2010): no. http://dx.doi.org/10.1002/chin.199113246.

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Divya, V., S. Biju, R. Luxmi Varma, and M. L. P. Reddy. "Highly efficient visible light sensitized red emission from europium tris[1-(4-biphenoyl)-3-(2-fluoroyl)propanedione](1,10-phenanthroline) complex grafted on silica nanoparticles." Journal of Materials Chemistry 20, no. 25 (2010): 5220. http://dx.doi.org/10.1039/c0jm00588f.

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Kowalska-Kuczyńska, Andrea, Jerzy Sokołowski, Małgorzata Iwona Szynkowska-Jóźwik, et al. "Evaluation of the Selected Mechanical and Aesthetic Properties of Experimental Resin Dental Composites Containing 1-phenyl-1,2 Propanedione or Phenylbis(2,4,6-trimethylbenzoyl)-phosphine Oxide as a Photoinitiator." International Journal of Molecular Sciences 24, no. 6 (2023): 5573. http://dx.doi.org/10.3390/ijms24065573.

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The goal of this study was to compare the mechanical properties of experimental resin dental composites containing a conventional photoinitiating system (camphorquinone CQ and 2-(dimethylami-no)ethyl methacrylate (DMAEMA)) to a photoinitiator system containing 1-phenyl-1,2 propanedione (PPD) with 2-(dimethylami-no)ethyl methacrylate) or acting alone phenylbis(2,4,6-trimethylbenzoyl)-phosphine oxide (BAPO). The manually produced composites consisted of an organic matrix: bis-GMA (60 wt. %), TEGDMA (40 wt. %), and silanized silica filler (45 wt. %). The composites contained 0.4/0.8 wt. %, 0.8/1.
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36

Pan, Min-Hsiung, Yi-Hong Sin, Ching-Shu Lai, et al. "Induction of Apoptosis by 1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione through Reactive Oxygen Species Production, GADD153 Expression, and Caspases Activation in Human Epidermoid Carcinoma Cells." Journal of Agricultural and Food Chemistry 53, no. 23 (2005): 9039–49. http://dx.doi.org/10.1021/jf051476a.

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37

Ainscough, Eric W., Andrew M. Brodie, Roger J. Cresswell та Joyce M. Waters. "Synthetic, spectroscopic, and X-ray crystallographic studies on the uranyl(VI) complexes of the β-diketophenol ligands 1-(2-hydroxyphenyl)-1,3-butanedione and 1-(2-hydroxyphenyl)-3-phenyl-1,3-propanedione". Inorganica Chimica Acta 277, № 1 (1998): 37–45. http://dx.doi.org/10.1016/s0020-1693(97)06094-5.

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38

Woods, J. A. O., H. Oluwatola Omoregie, N. Retta, Y. Chebude, and F. Capitelli. "Synthesis and Physicochemical Studies of Nickel(II) Complexes of 2-substituted-1,3-diphenyl-1,3-propanedione, their 2,2′-Bipyridine and 1,10-Phenanthroline Adducts and X-Ray Structure of (2,2′-Bipyridine)Bis(1,3-diphenyl-1, 3-propanedionato) Nickel(II)." Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry 39, no. 10 (2009): 694–703. http://dx.doi.org/10.1080/15533170903433220.

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39

Ingale, Ajit P., Santosh T. Shinde, and Nitin M. Thorat. "Sulfated tungstate: A highly efficient, recyclable and ecofriendly catalyst for synthesis of Flavones under the solvent-free conditions." Current Chemistry Letters 13, no. 3 (2024): 603–10. http://dx.doi.org/10.5267/j.ccl.2024.1.006.

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Sulfated tungstate efficiently catalyzes the cyclodehydration of 1-(2-hydroxyphenyl)-3-aryl-1,3-propanediones to flavones under solvent-free conditions. Utilization of conventional heating, simple reaction conditions, short reaction time, ease of product isolation and purification makes this manipulation very interesting from an economic and environmental perspective. Under these conditions, twelve examples were obtained with good yields (85-94%).
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40

Lee, Jae-In, and Se-Bin Park. "An Effective Synthesis of 3-Methoxyflavones via 1-(2-Hydroxyphenyl)-2-methoxy-3-phenyl-1,3-propanediones." Bulletin of the Korean Chemical Society 33, no. 4 (2012): 1379–82. http://dx.doi.org/10.5012/bkcs.2012.33.4.1379.

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41

Cuihong, Zhang, Ge Yuan, Huo Xiaoping, Yang Liguo, Li Xin та Miao Zongcheng. "Crystal structure of tris(1-phenyl-1,2-propanedione-2-oximato-κ2N,O)cobalt(III), C27H24N3O6Co". Zeitschrift für Kristallographie - New Crystal Structures 234, № 3 (2019): 473–74. http://dx.doi.org/10.1515/ncrs-2018-0479.

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AbstractC27H24N3O6Co, monoclinic, P21/c (no. 14), a = 11.309(3) Å, b = 19.477(5) Å, c = 11.615(3) Å, β = 109.071(9)°, V = 2418.0(11) Å3, Z = 4, Rgt(F) = 0.0296, wRref(F2) = 0.0845, T = 293(2) K [1–3].
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42

Öhlinger, Stefan Holger. "AN EFFICIENT SYNTHESIS OF β-(3-QUINOLINYL)-α-ALANINE". SOUTHERN BRAZILIAN JOURNAL OF CHEMISTRY 17, № 17 (2009): 1–8. http://dx.doi.org/10.48141/sbjchem.v17.n17.209.4_2009.pdf.

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A convenient synthesis for β-(3-quinolinyl)-α-alanine (4) is presented. Condensation of 2-chloro-3-chloromethylquinoline (5) with diethyl acetamidomalonate (2) gave high yield of diethyl 2-acetylamino-2-(2-chloro-3-quinolinylmethyl)- propanedionate (6), which was dehalogenated in the presence of ammonium formate and palladium/charcoal. Diethyl 2-acetamido-2-(3-quinolinylmethyl)-malonate (3) was easily converted to the amino acid. The condensation reaction between 2 and 6 is also useful for the construction of (1H)-2,3-dihydropyrrolo[2,3-b]quinoline-2,2-bis(carboxylic acid) and pyrrolo[2,3-b]qu
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Hageman, Hendrik J., and Pieter Oosterhoff. "Photoinitiators and photoinitiation, 16. The photodecomposition of some 1-phenyl-3-sulphonyloxy-1,2-propanediones." Macromolecular Chemistry and Physics 201, no. 14 (2000): 1687–90. http://dx.doi.org/10.1002/1521-3935(20000901)201:14<1687::aid-macp1687>3.0.co;2-m.

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44

R., N. Prasad, Gupta Seema, and Jangir Sarita. "Synthesis and characterization of MgII, CaII, SrII and BaII complexes of 2, 15-dimethyl-3, 16-diethyl/propyl/phenyl-1 ,4, 14,17 -tetraazacyclohexacosa- 1,3,14,16-tetraene." Journal of Indian Chemical Society Vol. 88, May 2011 (2011): 653–57. https://doi.org/10.5281/zenodo.5769024.

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Department of Chemistry, University of Rajasthan, Jaipur-302 055, Rajasthan, India <em>E-mail</em> : rnp _1949@yahoo.co.in <em>Manuscript received 02 September 2008, revised 08 September 2010, accepted 15 September 2010</em> 2+2 Cyclocondensation reactions of 1,9-diaminononane with a-diketones viz. 2,3-pentanedione, 2,3-hexanedione or 1-phenyl-1,2-propanedione in the presence of metal ions as templates have afforded hexacoordinated complexes of the general formula [MLX<sub><sup>2</sup></sub>] (where M = Mg, Ca, Sr or Ba; L = N<sub>4</sub> macrocycle having 26-membered ring and X = Cl or NCS).
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45

Unde, Pradip J., Nitin M. Thorat, and Limbraj R. Patil. "Microwave Assisted Efficient Synthesis of Flavone using ZnO Nanoparticles as Promoter under Solvent-Free Conditions." Asian Journal of Chemistry 31, no. 5 (2019): 1133–36. http://dx.doi.org/10.14233/ajchem.2019.21873.

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A simple and highly efficient protocol for synthesis of flavones from 1-(2-hydroxyphenyl)-3-aryl-1,3-propanediones in presence of ZnO nanoparticles as a promoter in thermal as well as microwave irradiation under solvent-free conditions have been demonstrated. The catalyst is inexpensive, stable, can be easily recycled/reused for several cycles with consistent activity and observed almost same yield confirming the stability of the catalyst. It is believed that the present approach will become an alternative route for the conventional reactions. Because in this protocol, yield is quite high, sho
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Nishinaga, Akira, Kazushige Maruyama, Hiroyuki Ando, et al. "Cobalt schiff base complex promoted retro-claisen reaction of 1-(2-hydroxyphenyl)-3-phenyl-1,3-propanediones and flavone formation." Tetrahedron Letters 31, no. 22 (1990): 3171–74. http://dx.doi.org/10.1016/s0040-4039(00)94724-5.

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47

Marin-Astorga, Norman, Gina Pecchi, and Patricio Reyes. "Ordered mesoporous silicates of MCM-41 type as support of pt catalysts for the enantioselective hydrogenation of 1-phenyl-1,2-propanedione." Reaction Kinetics and Catalysis Letters 87, no. 1 (2005): 121–28. http://dx.doi.org/10.1007/s11144-006-0017-3.

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48

Buceta, N. N., C. O. Della Védova, G. P. Romanelli, J. C. Autino, and J. L. Jios. "Deuterium isotopic effect on 13C NMR chemical shifts of 1-(2-hydroxyphenyl)-3-aryl-1,3-propanediones: Hydrogen bond and substituent effects." Journal of Molecular Structure 878, no. 1-3 (2008): 50–59. http://dx.doi.org/10.1016/j.molstruc.2007.07.032.

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NISHINAGA, A., K. MARUYAMA, H. ANDO, et al. "ChemInform Abstract: Cobalt Schiff Base Complex-Promoted Retro-Claisen Reaction of 1-(2- Hydroxyphenyl)-3-phenyl-1,3-propanedions and Flavone Formation." ChemInform 22, no. 26 (2010): no. http://dx.doi.org/10.1002/chin.199126105.

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Nakamura, Michio, Hisashi Okawa, Tasuku Ito, Masako Kato, and Sigeo Kida. "Nocovalent Interactions in Metal Complexes. 14. Proton NMR Spectroscopic Investigation on Stereoselectivity in Cobalt(III) Complexes of Various 3-Substituted 1-Phenyl-1,3-)propanediones." Bulletin of the Chemical Society of Japan 60, no. 2 (1987): 539–43. http://dx.doi.org/10.1246/bcsj.60.539.

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