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1 blackberry formation for a non-Mo-containing polyoxometalate.
2 ization of disulfide bond-based polymer with polyoxometalate.
3 ns, flexibility and dynamic is possible with polyoxometalates.
4 now facilitate efforts to design functional polyoxometalates.
5 ular metal-oxide nanoclusters, also known as polyoxometalates.
6 ner of the shell, evocative of mono-lacunary polyoxometalates.
7 s in selectivity in the self-assembly of the polyoxometalates.
8 of molecular oxygen in reactions mediated by polyoxometalates.
9 sport studies of magnetically functionalized polyoxometalates.
10 {P2 W18 } (3), and {Mo12 O36 (HPO3 )2 } (4) polyoxometalates.
12 (31)P NMR shows that the Cu-NO2-substituted polyoxometalates act as oxygen donors to the C-C double
13 irst, we reveal that the Anderson-Evans type polyoxometalate [AlMo(6)O(18)(OH)(6)](3-) represents an
15 sembled monolayer to enhance the doping with polyoxometalate, an impressive efficiency of 20.1 % is a
16 brid of silica aerogel with a Preyssler-type polyoxometalate and MIL-101(Cr) metal-organic framework
18 synthesised a pyridyl-capped Anderson-Evans polyoxometalate and used it to fabricate single-molecule
20 r the screening and scale up of syntheses of polyoxometalates and manganese-based single-molecule mag
21 the process of the self-assembly of gigantic polyoxometalates and their subsequent molecular growth,
22 l and biological sciences, are a subclass of polyoxometalates and usually self-assemble in aqueous-ph
23 rt through different oxidation states of the polyoxometalate, and we report here an efficient three-s
24 table redox states (e.g., metalloporphyrins, polyoxometalates, and C60) is more particularly discusse
25 clude aluminum polycations, transition-metal polyoxometalates, and the actinyl peroxide clusters have
26 terials, including organometallic complexes, polyoxometalates, and the primary focus of this Perspect
27 2)Mo(18)O(62)](4-), and [S(2)W(18)O(62)](4-) polyoxometalate anions (POMs) and oxidation of water occ
28 including but not limited to combinations of polyoxometalate anions and redox-active cations, was con
30 show that equilibration reactions typical of polyoxometalate anions keep the pH of the system near 7
38 etical and experimental investigation of two polyoxometalate-based metal-organic frameworks (MOFs), [
45 porating phosphorus(III)-based anions into a polyoxometalate cage, a new type of tungsten-based uncon
48 we describe how building block libraries of polyoxometalates can be used to construct systems with i
50 ) in the presence of a bio-inspired Ru-based polyoxometalate catalyst to produce synzyme protocells (
52 munication describes a new method for the Pd/polyoxometalate-catalyzed aerobic olefination of unactiv
54 The review article goes beyond the realms of polyoxometalate chemistry and encompasses emerging resea
58 elope of both events and employ it for a new polyoxometalate cluster, Na6 [Mo120 Ce6 O366 H12 (H2 O)7
59 2+) ) around a rigid, spherical, 2.9-nm size polyoxometalate cluster, {Mo(132) }(42-) , is determined
61 amolecular assembly of a series of nanoscale polyoxometalate clusters (from the same one-pot reaction
62 is achieved by incorporating Anderson-Evans polyoxometalate clusters (POMs, MMo(6)O(24), M = Rh/Pt)
64 nd have many common building blocks; in fact polyoxometalate clusters are perhaps the largest non-bio
66 ese results demonstrate the promise of using polyoxometalate clusters as building blocks for tunable
67 hods for the grafting of peptide chains onto polyoxometalate clusters by the use of general activated
68 the ability to add delocalized electrons to polyoxometalate clusters can be incorporated into self-a
70 lecular nanostructures like coordination and polyoxometalate clusters is extremely time-consuming sin
75 plets are reconfigured into membrane-bounded polyoxometalate coacervate vesicles (PCVs) in the presen
78 articles (Ag-NPs) encapsulated in a tungsten polyoxometalate compound (POM) are embedded within the p
79 ns to produce an aqueous solution of reduced polyoxometalate compounds that can be used to generate p
80 nts, to the best of our knowledge, the first polyoxometalate-driven paradigm as an efficient method t
81 the polyoxometalate, forming heterometallic polyoxometalates, e.g., [SiCu(II)Fe(III)Ga(III)(H(2)O)(3
82 O(2) in the first coordination sphere of the polyoxometalate, forming heterometallic polyoxometalates
83 uced into the synthesis of a uranyl peroxide polyoxometalate formulated as K(32)(UO(2))(19)(O(2))(26)
85 racterization of an organic-inorganic hybrid polyoxometalate functionalized by a short link with a tr
87 as an active catalyst, and iron(II) and the polyoxometalate H(5)PMo(10)V(2)O(40) (POM-V2) were ident
89 at all structural sites in two isostructural polyoxometalates, [H(x)Nb(10)O(28)]((6-x)-) and [H(x)Ti(
92 molecular water oxidation catalysts based on polyoxometalates have been reported that combine the adv
96 elf-assembly of organo-functionalised hybrid polyoxometalates (hereafter referred to as hybrid POMs),
101 istic investigation elucidating the roles of polyoxometalates in POM-photoelectrode hybrid oxygen evo
102 hould aid in the exploitation of these giant polyoxometalates in solution for various applications.
104 enerally applicable strategy for integrating polyoxometalates into functional architectures and devic
107 nd composition suggests reaction pathways in polyoxometalate ions will be highly variable even within
108 Access to asymmetrically functionalized polyoxometalates is a grand challenge as it could lead t
109 ared by pretreatment of the aqua-coordinated polyoxometalates (L = H2O) with NO2 or are formed in sit
110 based on redox-active (vanadate(V)-centered) polyoxometalate ligands, Na10[Co4(H2O)2(VW9O34)2].35H2O
111 c hybrid molecule comprising two Dawson-type polyoxometalates linked by a 2,2'-bipyridine unit, which
112 ution or X SOL), characterized by lanthanide polyoxometalates (LnPOMs) as heavy atoms source, which c
113 very similar to the unique self-assembly of polyoxometalate macroanions into single-layer, spherical
114 onstruct complex chemical systems based upon polyoxometalates, manipulating the templating/self templ
115 demonstrating the crucial role played by the polyoxometalate metal oxide cluster as an intermediary i
116 g a terminal aromatic pyrene platform with a polyoxometalate Mn-Anderson cluster as linker, demonstra
117 nd {Mo(154-x)}, as well as the largest known polyoxometalate {Mo(368)}, with improved yield (up to 26
119 been achieved using the ruthenium-containing polyoxometalate molecular catalyst, [{Ru4O4(OH)2(H2O)4}(
120 Here we show that a molybdenum(VI) oxide 'polyoxometalate' molecular nanocluster containing two em
122 ized by linking ditopic amino functionalized polyoxometalate [N(C(4)H(9))(4)](3)[MnMo(6)O(18){(OCH(2)
123 avior of giant toroidal molybdenum blue-type polyoxometalate, namely, the {Mo(154)} species in the pr
125 inorganic hybrid complexes between CB[n] and polyoxometalates not only display a surprisingly high st
127 TiO(2) support and ammonium phosphotungstic polyoxometalate (NPW) clusters anchored with isolated Pt
128 ptor anion, alpha-SiV(V)W(11)O(40)(5-) (1, a polyoxometalate of the Keggin structural class), was use
130 and programmed assembly of a dumbbell-shaped polyoxometalate-organic hybrid molecule comprising two D
132 fter as (COD)Ir.POM(8-), where POM(9-) = the polyoxometalate, P2W15Nb3O62(9-)) under H2 is investigat
135 een applied to the study of the reduction of polyoxometalate [PMo12O40](3-) adsorbed at a boron doped
137 several nanometers (molecular clusters, i.e. polyoxometalates, polyoxocations, and metal-organic poly
138 ed, dimeric, ZrIV-substituted Lindqvist-type polyoxometalate (POM) (nBu4N)6[{(mu-MeO)ZrW5O18}2], (TBA
139 report the encapsulation of a Ni-containing polyoxometalate (POM) [Ni4 (H2 O)2 (PW9 O34 )2 ](10-) (N
140 f pure approximately 0.75 nm size molybdenum polyoxometalate (POM) anions on 25 mug ( approximately 0
141 SS), [60]fullerene (C60), and Lindqvist-type polyoxometalate (POM) are used as building blocks to con
142 as a nanohybrid material by using S-rGO with polyoxometalate (POM) as a cathode-active material for a
145 In this review we discuss the relevance of polyoxometalate (POM) chemistry to provide model objects
147 hybrid molecules containing a large anionic polyoxometalate (POM) cluster and two C6 and C16 alkyl c
149 nteract with the conjugate anion in W and Mo polyoxometalate (POM) clusters and gaseous mineral acids
152 eactions on Bronsted acid catalysts based on polyoxometalate (POM) clusters are described in terms of
155 om single-walled carbon nanotubes (SWNTs) to polyoxometalate (POM) clusters results in the spontaneou
156 he contribution of building blocks of Keggin polyoxometalate (POM) clusters to redox processes are ch
157 zation of a new class of hybrid Wells-Dawson polyoxometalate (POM) containing a diphosphoryl group (P
159 a representative series of Keggin and Dawson polyoxometalate (POM) films in contact with a metallic (
162 We observed the diffusion and aggregation of polyoxometalate (POM) ions in water by using liquid phas
164 and neodymium complexes with five different polyoxometalate (POM) ligands were structurally and spec
168 nd electrochemical properties of a series of polyoxometalate (POM) oxoclusters decorated with two bod
169 and the redox-active macrocyclic {P(8)W(48)} polyoxometalate (POM) produces a striking synergistic ef
171 ance fuel cells that are catalyzed solely by polyoxometalate (POM) solution without any solid metal o
173 cy of silicotungstic acid (H(4)SiW(12)O(40)) polyoxometalate (POM) toward the reaction between furfur
174 self-assembly of hydrophilic Keplerate-type polyoxometalate (POM) {Mo(72)Fe(30)} macroanions into si
175 anion size and charge allows the Keggin-type polyoxometalate (POM), [CuPW(11)O(39)](5-), a catalyst f
176 ecognition processes involving a Dawson-type polyoxometalate (POM), [P2W18O62](6-), a cationic electr
177 This strategy employs a single material, a polyoxometalate (POM), alpha(2)-[P(2)W(17)O(61)](10-), t
178 composed of layered double hydroxide (LDH), polyoxometalate (POM), and dioctadecyldimethylammonium.
179 Here, we present a strategy for synthesizing polyoxometalate (POM)-based coordination networks with u
180 osmotically driven crystal morphogenesis of polyoxometalate (POM)-based crystals is investigated, wh
181 driven self-assembly processes of a covalent polyoxometalate (POM)-based hybrid bearing remote terpyr
182 Wells-Dawson [alpha(2)-P(2)W(17)O(61)](10-) polyoxometalate (POM)-supported [Re(CO)(3)](+) complex c
183 ocation process of countercations around one polyoxometalate(POM)-organic hybrid anionic cluster at v
187 drogen-bonded organic frameworks (HOFs), and polyoxometalates (POMs) are emerging PEM materials, offe
190 Predicting the number of electrons that polyoxometalates (POMs) can store, and whether these ele
192 a host-guest hybrid redox material based on polyoxometalates (POMs) encapsulated within the internal
201 of mononuclear lanthanoid complexes based on polyoxometalates (POMs) that exhibit single-molecule mag
202 peroxoniobium compounds to the corresponding polyoxometalates (POMs), alpha(1)-K(7)[P(2)W(17)NbO(62)]
203 ron oxides, previous Fe(III) -oxo cages, and polyoxometalates (POMs), hints that much larger molecula
204 ped to describe the energy landscapes of six polyoxometalates (POMs), Li-U(24), Li-U(28), K-U(28), Li
206 , enzymes, ...) and inorganic molecules like polyoxometalates (POMs), which have very interesting app
207 have been demonstrated for the first time in polyoxometalates (POMs), with an arylimido-derivative sh
208 Three organic-inorganic hybrid Mn-Anderson polyoxometalates (POMs), with both symmetrical and asymm
209 ters, Ir-based bridging ligands, and W-based polyoxometalates (POMs)-as a multifarious radioenhancer.
212 catalyst hypothesis: (i) six vanadium-based polyoxometalate precatalysts, (n-Bu4N)4H5PV14O42, (n-Bu4
213 that enables the incorporation of a platinum-polyoxometalate (Pt-POM) CH(4) oxidation precatalyst int
217 chromophores and deca-anionic tetraruthenate polyoxometalates (Ru(4)POM) as water oxidation catalysts
218 is performed by employing the tetraruthenate polyoxometalate [Ru(4)(mu-O)(4)(mu-OH)(2)(H(2)O)(4)(gamm
219 l fibre with the exposed tip coated with the polyoxometalate salt [(C(4)H(9))(4)N](4)H[PMo(10)V(2)O(4
220 d-loop exploration of the chemical space for polyoxometalate-scaffolding metal-organic frameworks (PO
222 of 10-20 nm by post-process immersion into a polyoxometalate solution (phosphomolybdic acid, PMA) in
223 mputationally, while the intricate nature of polyoxometalate speciation is best captured by adjusting
225 rected assembly of a ring-shaped macrocyclic polyoxometalate structural building unit, {P(8)W(48)O(18
226 ew method to identify metallic nanoclusters (polyoxometalate structures) in solution at the single mo
227 ation to minimize steric clashes between the polyoxometalate subunits, in order to stabilize the corr
229 s, is described using copper(II)-substituted polyoxometalates, such as {alpha2-Cu(L)P2W17O61}(8-) or
230 sights to those questions with a solubilized polyoxometalate-supported single-atom catalyst which all
233 ates can be obtained through the Keggin-type polyoxometalate-templated growth of a layer of spherical
234 of them known to date are negatively charged polyoxometalates, there is only a handful of cationic on
235 in the reaction mechanism by protonating the polyoxometalate thereby enabling the activation of the m
237 id growth of tubes occurs from crystals of a polyoxometalate upon addition of an aqueous solution con
238 g aromatic ketones, xanthene dyes (Eosin Y), polyoxometalates, uranyl salts, a metal-oxo porphyrin an
239 999, a catechol dioxygenase derived from a V-polyoxometalate was reported which was able to perform a
241 hat SMOF-1 adsorbs anionic Wells-Dawson-type polyoxometalates (WD-POMs) in a one-cage-one-guest manne
242 and water activation on multi-Ru-substituted polyoxometalates were studied using the B3LYP density fu
243 r for small-molecule activation with reduced polyoxometalates, where both electron and proton origina
244 u(+) and Bu3Sn(+) cations coordinated to the polyoxometalate, which were also identified by ESI-MS.
245 y of ([UO2(O2)OH]60)(60-) (U60), an actinide polyoxometalate with fullerene topology, can be induced
246 The technique allows the measurement of polyoxometalates with over 2 orders of magnitude lower a
247 self-assembly of an equilibrated ensemble of polyoxometalates, with the heteropolytungstate anion [AI
249 contrast agent, zirconium-substituted Keggin polyoxometalate (Zr-POM), the soft tissue of the placent