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1 MOF-525-J33 with 15.6 angstrom inter active-site distanc
2 MOFs synthesized with rare-earth (RE) elements, which in
3 MOFs with intrinsic thermocatalytic activity, as hosts f
5 MOF-808 can produce up to 8.66 L(H2O) kg(-1)(MOF) day(-1), an extraordinary finding that outperforms
8 articles (NPs) embedded in a Zr-based UiO-67 MOF was subject to steady-state and transient kinetic st
11 e of practical, rather than purely academic, MOF developments in the increasingly critical field of e
12 Here, we show that histone acetyltransferase MOF plays a critical role in this process through direct
13 us MOFs, monolayer MOF nanosheets, amorphous MOF liquids and glasses, polymers, metal nanoparticles,
14 n encoded in the newly formed SBUs drives an MOF-to-MOF conversion into bipartite nets compatible wit
16 ps of Zr(6)O(8) nodes in the MOFs UiO-66 and MOF-808, which have different densities of vacancy sites
17 nships among these groups, node defects, and MOF stability, and how do reaction conditions influence
18 wis acid-base interaction), between F(-) and MOF host, a highly selective, sensitive, and reliable fl
22 ein, the excitation bands of ytterbium-based MOFs are extended to 800 nm via the postsynthetic coupli
24 s, to study and clarify interactions between MOFs and biological milieu, human whole blood plasma was
25 The impact of this concept on "breathing" MOFs is discussed. I(2) sorption, both from gas phase an
29 ional modes, can be observed for carboxylate MOFs by monitoring the red-shifts of carboxylate stretch
31 A new cobalt metal-organic framework (2D-Co-MOF) based on well-defined layered double cores that are
34 electrode modified with a film of conductive MOF (M(3)HXTP(2); M = Ni, Cu; and X = NH, 2,3,6,7,10,11-
38 ined data in the current study, the designed MOF can be introduced as a new desirable carrier for dru
40 o enhance the efficiency of electrocatalytic MOFs should also consider other important kinetic parame
42 ve the CO selectivity from 74% for Ag/Zr-fcu-MOF-1,4-benzenedicarboxylic acid (BDC) to 94% for Ag/Zr-
44 show that the thermostabilities of ferritin-MOFs can be tuned through the metal component or the pre
45 eraging the synthetic modularity of ferritin-MOFs, we investigated the temperature-dependent structur
51 demonstrate superior accuracy especially for MOFs with high surface area (i.e., S(BET) over ~3000 m(2
52 boxylate (BTC(3-) ) ligand reagents, to form MOF nanocrystals, and collect and characterise them on a
53 framework aperture (metal-organic framework (MOF) = variable; guest = constant) was probed for the fi
54 (2) -MIL-125(Ti), a metal-organic framework (MOF) constructed from TiO(x) clusters and 2-aminoterepht
56 erately design a Th-metal-organic framework (MOF) for highly efficient separation of C(2)H(4) from a
59 ein we report how a metal organic framework (MOF) synthetic route can be optimized using an in situ m
60 K-1, a water-stable metal-organic framework (MOF) with 1-D channels, was synthesized in basic water.
61 on of an iron-based metal-organic framework (MOF) yielded well-dispersed pyrite FeS(2) nanoparticles
62 s of a water-stable metal-organic framework (MOF), Fe-HAF-1, constructed from supramolecular, Fe(3+)-
63 ligand Zr(IV)-based metal-organic framework (MOF),with underlying fcu topology, encompassing the [Zr(
66 materials, such as metal-organic frameworks (MOF), has been extensively investigated over the past fe
67 ostmodification of metal organic frameworks (MOFs) affords exceedingly high surface area materials wi
68 nd modular nature, metal-organic frameworks (MOFs) are an excellent platform material for systematica
71 orous, crystalline metal-organic frameworks (MOFs) are examined with regard to recent benchmark resul
75 layered conductive metal-organic frameworks (MOFs) as drop-casted film electrodes that facilitate vol
77 sis of ultraporous metal-organic frameworks (MOFs) based on metal trinuclear clusters, namely, NU-150
79 tigate a family of metal-organic frameworks (MOFs) containing triazolate linkers, M(2) X(2) (BBTA) (M
81 de perovskites and metal-organic frameworks (MOFs) has generated a new family of porous composite mat
82 rically conductive metal-organic frameworks (MOFs) has led to applications in chemical sensing and el
83 In that sense, metal-organic frameworks (MOFs) have been utilized to assemble unpreceded concentr
85 Semiconductive metal-organic frameworks (MOFs) have emerged in applications such as chemical sens
86 porous materials, metal-organic frameworks (MOFs) hold substantial promise as adsorbents for highly
88 e heterobimetallic metal-organic frameworks (MOFs) is now achieved by polymerization of molecular Ru(
92 her development of metal-organic frameworks (MOFs) requires an establishment of hierarchical interact
93 ctures inherent to metal-organic frameworks (MOFs) together with the facile tunability of their prope
94 namic stability of metal-organic frameworks (MOFs) using a model set of eight isostructural zeolitic
98 ncapsulated inside metal-organic frameworks (MOFs), thereby allowing us to improve CO(2)RR electrocat
99 ased on sulfonated metal-organic frameworks (MOFs), UiO-66-X, X = SAG, NH-SAG, (NH-SAG)(2) (SAG: sulf
100 carboxylate-based metal-organic frameworks (MOFs), we present general evidence that challenges the c
107 r work opens an avenue to develop functional MOF channels for selective ion conduction and efficient
112 The resulting crystalline heterobimetallic MOFs are solid solutions of Ru(2) and Cu(2) sites housed
113 ion spectra of a two-fold interpenetrated Hf MOF, linked by 1,4-phenylene-bis(4-ethynylbenzoate) liga
114 more exposed active sites of this design, HP-MOFs exhibited an enhanced catalytic efficiency in styre
117 In addition, the discovery of the new RE-hpt-MOF-1 and RE-ken-MOF-1 families of MOFs highlights the g
118 of several tens of thousands of hypothetical MOFs are evaluated at various thermodynamic conditions u
119 but dynamic bonding would explain important MOF phenomena in catalysis, postsynthetic exchange, nega
122 nected pores for efficient ion conduction in MOF/IL blends, whereas pore symmetry is a less stringent
126 anic qubit candidates have been installed in MOFs despite their structural variability and promise fo
129 l engineering of multiple catalytic sites in MOFs thus presents a unique opportunity to address outst
132 od enables the good dispersion of individual MOF nanoparticles on a spiderweb-like network within eac
133 haracterization tools, which can interrogate MOFs under realistic synthesis as well as catalysis (or
135 directs the formation of new RE-MOFs, RE-ken-MOF-1 (RE: Y(3+), Ho(3+), Er(3+), Yb(3+)), that display
136 discovery of the new RE-hpt-MOF-1 and RE-ken-MOF-1 families of MOFs highlights the great opportunitie
138 emonstrate that high conductivity in layered MOFs does not necessarily require a metal-ligand bond wi
139 d NH-linked analogs, CoPc-based and O-linked MOFs have lower activation energies in the formation of
140 ward the further practical application of Ln-MOF-based luminescent thermometers in various fields and
141 and temperature sensing behaviour of the Ln-MOF powder but also excellent mechanical properties, suc
142 ure and is water stable, highlighting FeNi-M'MOF as a promising material for C(2) H(2) /CO(2) separat
147 f of concept, the capacity to utilize the Mn-MOF for electrochemical CO(2) fixation and to spectrosco
148 e manganese 1,4-benzenedicarboxylate (MnBDC) MOFs with a precise control over their morphology (bulk
149 on and emission properties of these modified MOFs are maintained in the biological conditions of cell
150 ine)(3) ](NO(3) )(2) , CMOM-1S, is a modular MOF; five new variants in which counterions (BF(4) (-) ,
151 luding hierarchically porous MOFs, monolayer MOF nanosheets, amorphous MOF liquids and glasses, polym
153 that metal-organic framework nanoparticles (MOF NPs) densely functionalized with oligonucleotides ca
154 the synthesis and characterization of a new MOF prepared with the use of bismuth and dithieno[3,2-b:
155 , we employed net-clipping to form three new MOFs built with zigzag ligands, each of which exhibits t
156 ction as model, our strategy exploits the NP@MOF interface to create a pseudo high-pressure CO(2) mic
157 c substrate in this study is fixed at the NP@MOF interface to facilitate spectroscopic investigations
159 first briefly summarizes this background of MOF nanoparticle catalysis and then comprehensively revi
160 werful tools for initial characterization of MOF materials and for studying processes of their intera
164 how that these variations in the enthalpy of MOF formation are in linear correlation to the readily a
169 -1s surface, so the possible interactions of MOF-1s with fibrinogen also studied using fluorescence s
170 s, understanding the fundamental kinetics of MOF-based molecular catalysis of electrochemical reactio
171 of Fe atoms centered in porphyrin linkers of MOF sets the first protective barrier to inhibit the Fe
173 MOF layer on anode and filling the pores of MOF with hydrophobic Zn(TFSI)(2) -tris(2,2,2-trifluoroet
174 um frameworks by metal-exchange reactions of MOF crystals at temperatures below those conventionally
177 , in the first instance, the cytotoxicity of MOFs (particularly those used for various biological app
178 he dynamics of PSM can support the design of MOFs with increasingly sophisticated architectures.
179 eview, recent advances in the development of MOFs for separation of selected groups of hydrocarbons a
180 ew RE-hpt-MOF-1 and RE-ken-MOF-1 families of MOFs highlights the great opportunities existing in RE-M
181 teen lanthanides are an intriguing family of MOFs from the standpoint of both structure and function.
184 er, solid CH(4) storage in confined pores of MOFs in the form of hydrates is yet to be discovered.
188 the well-established designer properties of MOFs and, therefore, increase the scope of possibilities
189 undoubtedly the most studied key property of MOFs, that allows the protection of active biomolecules
190 significant progress made on this series of MOFs since 2018 is summarized and an update on the curre
191 e underline the MIL-, UiO- and ZIF-series of MOFs which remain until now the most used materials in d
193 the O(2) affinity at the open metal sites of MOFs for applications involving the strong and/or select
195 To further enrich the synthetic toolkit of MOFs, we report a controlled photolytic removal of linke
197 review highlights the advances in the use of MOFs in the elimination (adsorption and/or degradation)
198 methods should be applicable to a variety of MOFs, and scaling up synthesis possible via arrays of na
200 to get well-defined single site catalyst on MOF inorganic secondary building units, in particular th
201 nce in the next years concerning research on MOFs, to see if some of these materials may reach the en
202 w is expected to provide a timely summary on MOFs based on group 3 and 4 metals, which shall guide th
203 mples of delivery of multiple drugs from one MOF are rare, potentially hampered by difficulties in po
207 al sites in the acs net are retained in pacs MOFs; two thirds are used for pore-space partition.
208 way for the design and synthesis of periodic MOFs affording very efficient and fast ET to mimic natur
210 tm and 298 K, more than twice that of peroxo-MOF-74-Fe, has been achieved even though the isosteric h
211 ion potentials have not yet surpassed peroxo-MOF-74-Fe, these robust CPMs exhibit outstanding propert
214 re then crosslinked into a MOF-polythiourea (MOF-PTU) composite material, maintaining the catalytic p
215 ng materials including hierarchically porous MOFs, monolayer MOF nanosheets, amorphous MOF liquids an
217 industrial limitations of typically powdered MOFs are discussed while recent breakthroughs in MOF pro
218 heir unique tripartite construction, protein-MOFs possess extremely sparse lattice connectivity, sugg
219 ed protein-metal-organic frameworks (protein-MOFs) as chemically designed protein crystals, composed
220 These values are the highest among all RE MOFs based on nonanuclear clusters and some of the highe
221 eport a series of mesoporous rare-earth (RE) MOFs that are constructed from an unusual 12-connected p
222 ights the great opportunities existing in RE-MOFs in terms of structural diversity that could lead to
223 edral linker directs the formation of new RE-MOFs, RE-ken-MOF-1 (RE: Y(3+), Ho(3+), Er(3+), Yb(3+)),
229 thermoplastic dispersal of a semiconductive MOF (SCU-13) through a commercially available polymer, p
234 unt of methane stored in the pores of Cr-soc-MOF-1 in the form of MH was found to be ~50% larger than
237 ut this review), and shows that for standard MOFs based on metals already present in active molecules
250 first quantifiable relationship between the MOF thermodynamics and the linker structure, suggesting
251 analytical method was achieved, despite the MOF-functionalized probe approach being ~40 times quicke
253 We directly image defect nanodomains in the MOF UiO-66(Hf) over an area of ca. 1000 nm and with a sp
257 M is encapsulated within the cavities of the MOF by in situ synthesis, and then, the Rh catalytic com
258 of the MOF, magnetometry measurements of the MOF containing only N-oxide pillars demonstrated magneti
260 th both the calculated binding energy of the MOF for PFOA and the relative change in the surface area
262 ntrol over the nanoparticle synthesis of the MOF, HKUST-1, is achieved using a nanopipette injection
263 solvent removal causes decomposition of the MOF, magnetometry measurements of the MOF containing onl
264 of the POM in the octahedral cavities of the MOF: one at the center of a UiO-67 pore with the Cp*Rh c
265 protein showed the maximum frequency on the MOF-1s surface, so the possible interactions of MOF-1s w
266 synthesis and are distributed throughout the MOF at defect sites by coordination to the metal cluster
267 s presented that can simultaneously tune the MOF loading, composition, spatial distribution, and conf
272 ities of OH groups of Zr(6)O(8) nodes in the MOFs UiO-66 and MOF-808, which have different densities
273 of Ag nanoparticles incorporated inside the MOFs with the increase of local CO(2) concentration.
274 drug to be postsynthetically loaded into the MOFs to yield nanoparticles loaded with cocktails of dru
276 situ Raman spectroscopy, we reveal that the MOFs are stable under operating conditions and that this
278 nd versatile coordination modes within these MOFs endow the framework with high chemical stability, d
279 electrolyte from Zn anode by coating a thin MOF layer on anode and filling the pores of MOF with hyd
285 Zn) and MUV-102(Cu), heterometallic titanium MOFs isostructural with archetypical solids such as MIL-
286 les the formation of heterometallic titanium MOFs not accessible under solvothermal conditions at hig
287 tablishes the importance of applying SOMC to MOF chemistry to get well-defined single site catalyst o
289 ed in the newly formed SBUs drives an MOF-to-MOF conversion into bipartite nets compatible with the c
290 with high precision, paving the way towards MOF lithography, which has enormous potential in sensing
292 ecting a presynthesized microporous UiO-type MOF to ozonolysis, to confer it with mesopores sufficien
293 0.085x V(p) - 0.013x V(p) (2) for cage-type MOFs and n(tot) = 0.076x V(p) - 0.011x V(p) (2) for chan
294 076x V(p) - 0.011x V(p) (2) for channel-type MOFs, where V(p) is the pore volume of corresponding MOF
296 particular, we highlight cases that utilize MOF instability to fabricate varying materials including
297 The work offers a further avenue to utilize MOFs in the pursuit of materials design for CO(2)RR.
298 ntrol efficient exciton displacements within MOFs, we first developed linkers with low electronic sym