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1 ents 2-phenylpyridinate, and acac represents acetylacetonate).
2 = bipyridine; en = ethlylenediamine; acac = acetylacetonate).
3 ety is either Pd(acac)2 or Pt(acac)2 (acac = acetylacetonate).
7 noncoordinating anion and beta-diketonate = acetylacetonate (acac), 1,1,1,-trifluoroacetylacetonate
9 ))(2)](OTf)(2) (where pyacac = 3-(4-pyridyl)-acetylacetonate and bpy' = 4,4'-5,5'-tetramethyl-2,2'-bi
10 uPt nanoparticles by coreduction of platinum acetylacetonate and copper acetylacetonate in the presen
11 e M/CuPd NPs by the coreduction of palladium acetylacetonate and copper acetylacetonate in the presen
12 FePt) nanoparticles by reduction of platinum acetylacetonate and decomposition of iron pentacarbonyl
13 alt oxazoline palladacycles (COP) containing acetylacetonate and hexafluoroacetylacetonate ligands we
14 -Pt nanocubes were synthesized from platinum acetylacetonate and manganese carbonyl in the presence o
15 (165)Ho-MSNs were prepared using (165)Ho-acetylacetonate and MCM-41 silica particles, and stabili
16 elated model compound Fe(III)(acac)3 (acac = acetylacetonate) and nearly 140-fold higher than an earl
17 mmonium hydroxide (TPAOH) and manganese(III)-acetylacetonate as organic template and manganese salts,
18 , bis(2-phenyl benzothiozolato-N,C2')iridium(acetylacetonate) [bt2Ir(acac)], and bis(2-(2'-benzothien
19 (2-(2'-benzothienyl)pyridinato-N,C3')iridium(acetylacetonate) [btp2Ir(acac)], were doped into the emi
22 um acetylacetonate, In(acac)(3), and tin bis(acetylacetonate)dichloride, Sn(acac)(2)Cl(2), at 270 deg
24 erature solution phase reaction of iron(III) acetylacetonate, Fe(acac)(3), with 1,2-hexadecanediol in
25 2-(2'-benzo[b]thienyl)pyridinato and acac is acetylacetonate) have been attached either directly (spa
26 ethylendiamine, gly = glycinate, and acac = acetylacetonate, have been synthezised and fully charact
27 ization, using the recently developed phenyl-acetylacetonate (i.e., phenyl-acac) anchor as a referenc
28 ction of platinum acetylacetonate and copper acetylacetonate in the presence of 5 nm Au nanoparticles
29 tion of palladium acetylacetonate and copper acetylacetonate in the presence of Ag (or Au) nanopartic
30 ynthesized by hydride reduction of manganese acetylacetonate in the presence of Au nanoparticles.
31 nthesized by thermal decomposition of indium acetylacetonate, In(acac)(3), and tin bis(acetylacetonat
32 ing materials, Pd(acac)2 and IPr.HCl [acac = acetylacetonate; IPr = N,N'-bis(2,6-diisopropylphenyl)im
33 O,O)2Ir(R)(L), R-Ir-L (acac-O,O = kappa2-O,O-acetylacetonate, -Ir- is the trans-(acac-O,O)2Ir(III) mo
35 ble resonance spectra revealed an equatorial acetylacetonate ligand, indicating that one of the organ
37 ing modes, the former being dominant for the acetylacetonate-linked chromophores, the latter for the
39 xture of Fe(acac)(3) and Ln(acac)(3) (acac = acetylacetonate; Ln = Sm, Eu, Gd) in the presence of pas
40 by solution-phase deposition of an iron(III) acetylacetonate molecular ink followed by sequential ann
41 magnetic relaxation agents, including nickel acetylacetonate (NiAA), nickel ethylenediaminediacetate
42 reaction with appropriate hydrated salts or acetylacetonates of Al(III), Fe(III), Ga(III), and In(II
43 ized by covalent attachment of 4-nitrophenyl-acetylacetonate or coumarin 343 adsorbates, exhibit hole
44 , i.e., bis(2-phenylpyridinato-N,C2')iridium(acetylacetonate) [ppy2Ir(acac)], bis(2-phenyl benzothioz
45 light in the presence of [Ir(acac)3] (acac: acetylacetonate) precursor followed by calcination under
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