ライフサイエンスコーパス: acetylacetonate

1 = bipyridine; en = ethlylenediamine; acac = acetylacetonate).

2 ents 2-phenylpyridinate, and acac represents acetylacetonate).

3 ety is either Pd(acac)2 or Pt(acac)2 (acac = acetylacetonate).

4 volution reaction using monolayers of cobalt(acetylacetonate)(2)bipyridine.

5 (+) to -6895 ppm of [1](-) (referenced to Rh(acetylacetonate)(3)).

6 d compared to the related compounds with the acetylacetonate (acac) ancillary ligand.

7 ketonates, with the major emphasis placed on acetylacetonate (acac) complexes.

8 olved in strong complexation equilibria with acetylacetonate (acac) ligands.

9 A novel class of derivatized acetylacetonate (acac) linkers for robust functionalizat

10 noncoordinating anion and beta-diketonate = acetylacetonate (acac), 1,1,1,-trifluoroacetylacetonate

11 Iron(II) acetylacetonate along with oxidant (K2S2O8) and phase-tr

12 ))(2)](OTf)(2) (where pyacac = 3-(4-pyridyl)-acetylacetonate and bpy' = 4,4'-5,5'-tetramethyl-2,2'-bi

13 e M/CuPd NPs by the coreduction of palladium acetylacetonate and copper acetylacetonate in the presen

14 uPt nanoparticles by coreduction of platinum acetylacetonate and copper acetylacetonate in the presen

15 FePt) nanoparticles by reduction of platinum acetylacetonate and decomposition of iron pentacarbonyl

16 alt oxazoline palladacycles (COP) containing acetylacetonate and hexafluoroacetylacetonate ligands we

17 -Pt nanocubes were synthesized from platinum acetylacetonate and manganese carbonyl in the presence o

18 (165)Ho-MSNs were prepared using (165)Ho-acetylacetonate and MCM-41 silica particles, and stabili

19 elated model compound Fe(III)(acac)3 (acac = acetylacetonate) and nearly 140-fold higher than an earl

20 mmonium hydroxide (TPAOH) and manganese(III)-acetylacetonate as organic template and manganese salts,

21 , bis(2-phenyl benzothiozolato-N,C2')iridium(acetylacetonate) [bt2Ir(acac)], and bis(2-(2'-benzothien

22 (2-(2'-benzothienyl)pyridinato-N,C3')iridium(acetylacetonate) [btp2Ir(acac)], were doped into the emi

23 Their Pt(II) acetylacetonate complexes have been synthesized and full

24 First-row transition metal acetylacetonate complexes, which have been characterized

25 um acetylacetonate, In(acac)(3), and tin bis(acetylacetonate)dichloride, Sn(acac)(2)Cl(2), at 270 deg

26 Reaction of the Schiff-base complex [Co(acetylacetonate-ethylenediimine)(NH3)2]+ with metmyoglob

27 ketoesters using commercially available iron acetylacetonate (Fe(acac)(2)) as a catalyst.

28 erature solution phase reaction of iron(III) acetylacetonate, Fe(acac)(3), with 1,2-hexadecanediol in

29 2-(2'-benzo[b]thienyl)pyridinato and acac is acetylacetonate) have been attached either directly (spa

30 ethylendiamine, gly = glycinate, and acac = acetylacetonate, have been synthezised and fully charact

31 Sodium acetylacetonate helps extract Cl(-) concomitant with the

32 ization, using the recently developed phenyl-acetylacetonate (i.e., phenyl-acac) anchor as a referenc

33 ction of platinum acetylacetonate and copper acetylacetonate in the presence of 5 nm Au nanoparticles

34 tion of palladium acetylacetonate and copper acetylacetonate in the presence of Ag (or Au) nanopartic

35 ynthesized by hydride reduction of manganese acetylacetonate in the presence of Au nanoparticles.

36 nthesized by thermal decomposition of indium acetylacetonate, In(acac)(3), and tin bis(acetylacetonat

37 ing materials, Pd(acac)2 and IPr.HCl [acac = acetylacetonate; IPr = N,N'-bis(2,6-diisopropylphenyl)im

38 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

39 Cobalt bis(acetylacetonate) is shown to mediate hydrogen atom trans

40 ble resonance spectra revealed an equatorial acetylacetonate ligand, indicating that one of the organ

41 The binding of carboxylate- and acetylacetonate-linked chromophores to homodisperse poly

42 ing modes, the former being dominant for the acetylacetonate-linked chromophores, the latter for the

43 Chromophores with acetylacetonate linking groups invariably bind in the ch

44 xture of Fe(acac)(3) and Ln(acac)(3) (acac = acetylacetonate; Ln = Sm, Eu, Gd) in the presence of pas

45 By reacting 2+ metal-acetylacetonate (M(acac)(2)) precursors in an amine solv

46 atment of ZIF-8 membranes with manganese(II) acetylacetonate (Mn(acac)(2) ) allows permselectivity tu

47 by solution-phase deposition of an iron(III) acetylacetonate molecular ink followed by sequential ann

48 magnetic relaxation agents, including nickel acetylacetonate (NiAA), nickel ethylenediaminediacetate

49 reaction with appropriate hydrated salts or acetylacetonates of Al(III), Fe(III), Ga(III), and In(II

50 ized by covalent attachment of 4-nitrophenyl-acetylacetonate or coumarin 343 adsorbates, exhibit hole

51 , i.e., bis(2-phenylpyridinato-N,C2')iridium(acetylacetonate) [ppy2Ir(acac)], bis(2-phenyl benzothioz

52 light in the presence of [Ir(acac)3] (acac: acetylacetonate) precursor followed by calcination under

53 modynamics of HAT from various ruthenium bis(acetylacetonate) pyridine-imidazole complexes to nitroxy

54 Herein we demonstrate that vanadium(III) acetylacetonate (V(acac)(3) ) is an efficient soluble ca

55 de by the reaction of Rh(eta(2)-C(2)H(4))(2)(acetylacetonate) with the support and anchored by two Rh