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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
4                      At present, over 90,000 MOFs have been synthesized and over 500,000 predicted.
5 MOF-808 can produce up to 8.66 L(H2O) kg(-1)(MOF) day(-1), an extraordinary finding that outperforms
6                            The utility of 2D MOFs in voltammetric sensing is measured by the detectio
7 thanide (Ln(3+)) materials, including Ln(3+) MOFs and Ln(3+) salts.
8 articles (NPs) embedded in a Zr-based UiO-67 MOF was subject to steady-state and transient kinetic st
9         The MOFs are then crosslinked into a MOF-polythiourea (MOF-PTU) composite material, maintaini
10 tradeoff between the catalytic activity of a MOF and its resistance to unzipping.
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
15 the largest Forster distances observed in an MOF.
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
19 ic acid) (pbdc) polymers in two archetypical MOF lattices (UiO-66 and IRMOF-1).
20 o tailor the size and shape of peptide-based MOF single crystals to specific applications.
21 Here, we report a series of lanthanide-based MOFs that allow fine tuning of the sheet stacking.
22 ein, the excitation bands of ytterbium-based MOFs are extended to 800 nm via the postsynthetic coupli
23                          The linkage between MOF and tumor proliferation suggests that there are addi
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
26 ap while it has no observable effect on bulk MOFs.
27       Conductive metal-organic frameworks (c-MOFs) have drawn increasing attention for their outstand
28          However, the majority of reported c-MOFs are based on 2D structures.
29 ional modes, can be observed for carboxylate MOFs by monitoring the red-shifts of carboxylate stretch
30  to screen 1632 experimentally characterized MOFs.
31  A new cobalt metal-organic framework (2D-Co-MOF) based on well-defined layered double cores that are
32        Electrochemical activation of a 2D-Co-MOF@Nafion-modified graphite electrode in aqueous soluti
33 omparison with previously explored concepts (MOF = constant; guest = variable).
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-
35 view of outstanding challenges in conductive MOFs.
36 core in a family of isostructural conductive MOFs with Mn(2+) , Zn(2+) , and Cd(2+) .
37 ere V(p) is the pore volume of corresponding MOFs.
38 ined data in the current study, the designed MOF can be introduced as a new desirable carrier for dru
39           The analytical performance of each MOF for detecting PFOA was correlated with both the calc
40 o enhance the efficiency of electrocatalytic MOFs should also consider other important kinetic parame
41                         Upon laser exposure, MOF crystals shrank while metal oxide nanoparticles form
42 ve the CO selectivity from 74% for Ag/Zr-fcu-MOF-1,4-benzenedicarboxylic acid (BDC) to 94% for Ag/Zr-
43 dicarboxylic acid (BDC) to 94% for Ag/Zr-fcu-MOF-1,4-naphthalenedicarboxylic acid (NDC).
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
46               We report a family of flexible MOFs based on derivatized amino acid linkers.
47              The targeted design of flexible MOFs demands control over the macroscopic thermodynamics
48 ralayer space of two-dimensional fluorinated MOFs for capturing acetylene from ethylene.
49                                          For MOF chemists, the chemical design space is a combination
50 tperforms any previously reported values for MOF-based systems.
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
55 res of a conductive metal-organic framework (MOF) electrode under operating conditions.
56 erately design a Th-metal-organic framework (MOF) for highly efficient separation of C(2)H(4) from a
57  in a dual-function metal-organic framework (MOF) is reported.
58                     Metal-organic framework (MOF) nanoparticles, also called porous coordination poly
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(
64 adiation study of a metal-organic framework (MOF).
65 the first plutonium metal-organic framework (MOF).
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
69                    Metal-organic frameworks (MOFs) are an intriguing type of crystalline porous mater
70                    Metal-organic frameworks (MOFs) are appealing heterogeneous support matrices that
71 orous, crystalline metal-organic frameworks (MOFs) are examined with regard to recent benchmark resul
72                    Metal-organic frameworks (MOFs) are hybrid materials composed of metal ions and or
73                    Metal-organic frameworks (MOFs) are intriguing host materials in composite electro
74                    Metal-organic frameworks (MOFs) are promising materials for onboard hydrogen stora
75 layered conductive metal-organic frameworks (MOFs) as drop-casted film electrodes that facilitate vol
76 directly construct metal-organic frameworks (MOFs) as enzyme protective carriers is presented.
77 sis of ultraporous metal-organic frameworks (MOFs) based on metal trinuclear clusters, namely, NU-150
78             Porous metal-organic frameworks (MOFs) capable of storing a relatively high amount of dry
79 tigate a family of metal-organic frameworks (MOFs) containing triazolate linkers, M(2) X(2) (BBTA) (M
80 al conductivity in metal-organic frameworks (MOFs) has been an open question.
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
84                    Metal-organic frameworks (MOFs) have drawn wide attention as candidate catalysts,
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
87         Processing metal-organic frameworks (MOFs) into hierarchical macroscopic materials can greatl
88 e heterobimetallic metal-organic frameworks (MOFs) is now achieved by polymerization of molecular Ru(
89                    Metal-organic frameworks (MOFs) offer a high potential for this application due to
90 for elaboration of metal-organic frameworks (MOFs) post-synthesis.
91         Conductive metal organic frameworks (MOFs) represent a promising class of porous crystalline
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
95                    Metal-organic frameworks (MOFs) with coordinatively unsaturated metal sites are ap
96                    Metal-organic frameworks (MOFs), atomically precise hybrid materials that are synt
97                    Metal-organic frameworks (MOFs), constructed from organic linkers and inorganic bu
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
101          Recently, metal-organic frameworks (MOFs), which are crystalline coordination polymers with
102 ) into porphyrinic metal-organic frameworks (MOFs).
103  from multivariate metal-organic frameworks (MOFs).
104  key properties of metal-organic frameworks (MOFs).
105 lass of materials, metal-organic frameworks (MOFs).
106 ticles or extended metal organic frameworks (MOFs)/metal-carbon composites, etc.
107 r work opens an avenue to develop functional MOF channels for selective ion conduction and efficient
108  defects, or "microstructure", in functional MOF design.
109 ery and development of stable and functional MOFs for practical applications.
110 recent innovations of aptamer-functionalized MOFs-based biosensors and their bio-applications.
111                                Functionally, MOF is found in two distinct complexes: NSL (nonspecific
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
115 nker labilization for the construction of HP-MOFs have emerged.
116 e nanoparticles formed giving rise to the HP-MOFs.
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
120          However, despite recent advances in MOF-based electrocatalysis, so far no attempt has been m
121  are discussed while recent breakthroughs in MOF processing are highlighted.
122 nected pores for efficient ion conduction in MOF/IL blends, whereas pore symmetry is a less stringent
123 ls after the training of the ML algorithm in MOFs.
124                       Structural dynamics in MOFs, however, typically refers to the "breathing" behav
125 umber of Reviews have covered flexibility in MOFs.
126 anic qubit candidates have been installed in MOFs despite their structural variability and promise fo
127 cess the underlying free energy landscape in MOFs.
128  for characterizing adsorption mechanisms in MOFs.
129 l engineering of multiple catalytic sites in MOFs thus presents a unique opportunity to address outst
130 fer and inaccessibility of internal space in MOFs.
131 far to achieve efficient charge transport in MOFs.
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
134 sition dipoles) and then assembled them into MOFs.
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
137 hermodynamics of two flexible pillared-layer MOFs.
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
143 2) molecules and the binding sites of FeNi-M'MOF.
144                             Mechanistically, MOF/FAO inhibition acts through reducing mitochondrial r
145 ncorporation of large polymers in mesoporous MOFs.
146 nkers to create mesopores within microporous MOFs at tens of milliseconds.
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
152  within a complex cavity of a multicomponent MOF.
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
158 oughs and milestones realized in the area of MOF-based small-scale swimmers.
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
161                        Maternal depletion of MOF acetyltransferase leading to H4K16ac loss causes abe
162                  The spatial distribution of MOF functionalization reveals that postsynthetic modific
163                             Dysregulation of MOF activity occurs in multiple cancers, including ovari
164 how that these variations in the enthalpy of MOF formation are in linear correlation to the readily a
165           Moreover, zygotic re-expression of MOF was neither able to restore embryonic viability nor
166 uture research possibilities in the field of MOF characterization.
167 r to tailor the electrocatalytic function of MOF-anchored active sites at the molecular level.
168 gests that there are additional functions of MOF that remain to be discovered.
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
172 nce that challenges the common perception of MOF metal-linker bonds being static.
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
175 w, the recent advances in the application of MOFs in heterogeneous catalysis are discussed.
176  to predict the hydrogen storage capacity of MOFs with different pore geometries.
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.
182 me of the highest in the entire RE family of MOFs.
183                             Peculiarities of MOFs interaction with specific gases and some inconsiste
184 er, solid CH(4) storage in confined pores of MOFs in the form of hydrates is yet to be discovered.
185 " approach utilizes the inherent porosity of MOFs and host-guest interactions.
186 ed at selected crystallographic positions of MOFs promoted their photocatalytic efficiency.
187 thod for studying sorption depth profiles of MOFs.
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
192  learning method to quantify similarities of MOFs to analyse their chemical diversity.
193 the O(2) affinity at the open metal sites of MOFs for applications involving the strong and/or select
194                             The stability of MOFs is a key prerequisite for their potential practical
195   To further enrich the synthetic toolkit of MOFs, we report a controlled photolytic removal of linke
196 ed net-clipping to predict the topologies of MOFs containing zigzag ligands.
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
199             Single-crystal X-ray analyses on MOF-1 showed that Cu(+2) ion was 6-coordinated.
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
204                                The optimized MOF-sensor had a CN(-) -detection limit of 0.05 mum, whi
205 erning nucleation and growth mechanisms in p-MOF systems.
206                The structural evolution of p-MOFs was probed by cryo-transmission electron microscopy
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
209 as low as about one-third of that for peroxo-MOF-74-Fe (66.8 kJ/mol).
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
212 itions was constructed using a 5x5 pixelated MOF-based imager.
213 erves as the foundation for future plutonium MOF chemistry.
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
216        Importantly, DNA-modified porphyrinic MOF nanorods (PCN-222) were assembled into 2D superlatti
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+)),
224              First, diverse structures of RE-MOFs are presented, divided into classes based on the co
225                                    Recently, MOF materials, featuring high surface areas, rich struct
226                         Four water-resistant MOFs-ZIF-8, UiO-66, MIL88-A, and Tb(2)(BDC)(3)-were coat
227 ochromic molecules integrated inside a rigid MOF scaffold are discussed.
228 re trends on the structural design of robust MOFs with high connectivity is provided.
229  thermoplastic dispersal of a semiconductive MOF (SCU-13) through a commercially available polymer, p
230          However, examples of semiconductive MOFs within flexible electronics have not been reported.
231 inatively unsaturated metal sites of several MOF families.
232 empirical equations are validated by several MOFs with an average deviation of 5.4%.
233 on Cr-soc-MOF-1 vs smaller cavities of Y-shp-MOF-5.
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
235  experimental case study performed on Cr-soc-MOF-1 vs smaller cavities of Y-shp-MOF-5.
236       In this study, an exceptionally stable MOF catalyst consisting of Pt nanoparticles (NPs) embedd
237 ut this review), and shows that for standard MOFs based on metals already present in active molecules
238        The rational design of 3D structures (MOFs, COFs, etc.) is presently limited by our understand
239                                   Switchable MOFs are a type of smart material that undergo distinct,
240                              The synthesized MOF Azole-Th-1 shows a UiO-66-type structure with fcu to
241                 The findings allow tailoring MOF microstructure to application.
242                        We show how targeting MOFs toward mitochondria represents a valuable strategy
243                        The Zn(TFSI)(2) -TFEP@MOF electrolyte protected Zn anode enables a Zn||Ti cell
244           The present study underscores that MOFs are promising to develop artificial LHCs, but that
245                                          The MOF acetyltransferase-containing Non-Specific Lethal (NS
246                                          The MOF can be loaded with organic molecules by immersion in
247                                          The MOF encapsulated Zn(TFSI)(2) -TFEP forms a ZnF(2) -Zn(3)
248  integrity of the POM, the catalyst, and the MOF after catalysis.
249 der Waals interaction between ethane and the MOF skeleton.
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
252 gher than the number of open Zr sites in the MOF lattice around each Pt NP.
253  We directly image defect nanodomains in the MOF UiO-66(Hf) over an area of ca. 1000 nm and with a sp
254 sized to arise from diffusion rates into the MOF that are slower than linker exchange.
255  maintaining the catalytic properties of the MOF and the flexibility of the polymer.
256 guest interactions by chemical tuning of the MOF backbone.
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
259 NPs are well dispersed on the surface of the MOF crystals and have a narrow size distribution.
260 th both the calculated binding energy of the MOF for PFOA and the relative change in the surface area
261 e relative change in the surface area of the MOF upon exposure to PFOA.
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
268 veals that most of the void space within the MOF is accessible to the solvent.
269                                          The MOFs are grown on Si/SiOx substrates modified with an or
270                                          The MOFs are then crosslinked into a MOF-polythiourea (MOF-P
271 romine intercalation is possible between the MOFs layers for the first time.
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
275 dles for postsynthetic polymerization of the MOFs into functional materials.
276  situ Raman spectroscopy, we reveal that the MOFs are stable under operating conditions and that this
277                                        These MOF carriers can also serve as the disintegrating agents
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
280                                         This MOF shows not only a remarkable volumetric C(2) H(2) upt
281                                         This MOF-PTU hybrid material was spray-coated onto Nyco texti
282         The phyiscal characteristics of this MOF family are insensitive to changes in the metal catio
283 ntrinsic redox character endow the 2D Cu-THQ MOF with promising electrochemical activity.
284 density of conjugated pai-systems throughout MOF pores.
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
288 t have been reported for imparting motion to MOFs.
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
291 cture, suggesting a route to design and tune MOF stability.
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
295                Relative to other ultraporous MOFs, NU-1501-Al exhibits concurrently a high gravimetri
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
299                  A new layered mesoporous Zr-MOF of composition [Zr(30)O(20)(OH)(26)(OAc)(18)L(18)] w
300                             We found that Zr-MOF-808 can produce up to 8.66 L(H2O) kg(-1)(MOF) day(-1

 
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