ライフサイエンスコーパス: MOF

1 MOF-1201 shows a 100 times lower release rate compared w

2 MOFs may prove useful in the dissipation of shock wave e

3 MOFs represent the development of covalent chemistry "be

4 MOFs that have failed to be activated previously can ach

5 MOFs with widely varied fluorometric sensing properties

6 MOFs, constructed by the designed assembly of metal ions

7 tegrity and accessible porosity of CD-MOF-1 (MOF, metal-organic framework).

8 In total, we report 22 MOFs that vary in both composition and structure yet sha

9 methylphosphonate (DMMP), on UiO-66, UiO-67, MOF-808, and NU-1000 using synchrotron-based X-ray powde

10 0,11-hexaiminotriphenylene)2 (Ni3(HITP)2), a MOF with high electrical conductivity, can serve as the

11 highest reported ordering temperatures for a MOF.

12 edge, this represents the first example of a MOF capable of separating chiral polar drugs.

13 In the absence of a MOF, the expected Morita-Baylis-Hillman product, a beta-

14 res and internal diameters of 7.8 and 9.6 A (MOF-1201) and 4.6 and 5.6 A (MOF-1203), respectively.

15 7.8 and 9.6 A (MOF-1201) and 4.6 and 5.6 A (MOF-1203), respectively.

16 higher concentration of monocarboxylic acid MOFs were isostructural but suffered from increased fwhm

17 m and constructed the first indium-based alb-MOF, In-alb-MOF, by employing trinuclear [In3(mu3-O)(O2C

18 ucted the first indium-based alb-MOF, In-alb-MOF, by employing trinuclear [In3(mu3-O)(O2C-)6] as the

19 rmation of the first related alb-MOF, RE-alb-MOF.

20 ed to the formation of the first related alb-MOF, RE-alb-MOF.

21 Although MOF breathing can be inferred from the analysis of adsor

22 ptionally large range of pH resistance among MOFs.

23 construction of composite MOFs and amorphous MOFs, as well as providing new synthetic routes for MOF

24 n biomedical settings and the addition of an MOF coating opens the way for the sensing of volatile or

25 te metathesis and metal node extension in An-MOFs are reported, and the results of the former approac

26 In the presence of MOFs with UMCM-1 and MOF-5 topologies, the reaction is selective to Aldol-Tis

27 rategy is versatile to a variety of MNPs and MOF crystals.

28 lopments in the field of luminescent MOF and MOF-based photonic crystals/thin film sensory materials.

29 Herein, we shine light on CPs and MOFs as optical media for state-of-the-art photonic phen

30 hree- and multi-photon absorption in CPs and MOFs is further supplemented with application-oriented p

31 onlinear optical (NLO) properties of CPs and MOFs, with a closer look at the two-photon absorption pr

32 s and the synergistic effects of enzymes and MOFs.

33 c microporous materials such as zeolites and MOFs, a field of research that has emerged some 15 years

34 ne) acetyltransferase 8 (KAT8, also known as MOF) mediates the acetylation of histone H4 at lysine 16

35 present a mesoporous cationic thorium-based MOF (SCU-8) containing channels with a large inner diame

36 to transplant shp topology into copper-based MOFs by employing the copper paddlewheel [Cu2(O2C-)4] as

37 trakis(p-benzoic acid)pyrene; H4TBAPy)-based MOFs: ROD-7 (In2(OH)2TBAPy, frz), NU-901 (scu), and NU-1

38 chemical warfare agent simulants on Zr-based MOFs open new opportunities in rational design of new an

39 L-125, a TiO2/1,4-benzenedicarboxylate (bdc) MOF for the oxidation of benzyl alcohol to benzaldehyde

40 d H2S and NO detectors reported and the best MOF-based chemiresistive sensors for these analytes.

41 cyclo[2.2.2]octane dicarboxylic acid (BODCA)-MOF, a metal-organic framework (MOF) built with a high-s

42 he bicyclo[2.2.2]octane (BCO) group in BODCA-MOF constitutes an example where engineered rotational d

43 d with significantly increased risk for both MOF and hip fracture.

44 is similar to the mechanism behind breathing MOFs, but is unique because the deformation pattern exte

45 Zr6(mu3-O)4(mu3-OH)4(HCO2)6 nodes in Zr-BTC (MOF-808) to the [Zr6(mu3-O)4(mu3-OH)4Cl12](6-) nodes in

46 icle surface that is independent of the bulk MOF structure.

47 amage repair pathways that are controlled by MOF, as correlated with a significant increase in yH2AX

48 paving the way for the long-awaited (6,12)-c MOF with alb topology.

49 Attempts to obtain a CD-MOF containing only Li(+) ions resulted in nonporous mat

50 counting for the cation/gamma-CD ratio in CD-MOF-1.

51 on the part of the Li(+) ions in the new CD-MOF has been confirmed by single-crystal X-ray analysis

52 ural integrity and accessible porosity of CD-MOF-1 (MOF, metal-organic framework).

53 e capacities of the Li(+)-ion-substituted CD-MOF have been shown to exceed the highest sorption capac

54 t sorption capacities reported so far for CD-MOFs.

55 of carbohydrate metal-organic frameworks (CD-MOFs) in a combination of alkali-metal cations.

56 the Ca(2+) counterions of a preformed chiral MOF of formula Ca6(II){Cu(II)24[(S,S)-hismox]12(OH2)3}.2

57 Reported herein are two new polymorphic Co-MOFs (CTGU-5 and -6) that can be selectively crystallize

58 tructural integrity, as the parent cobaltous MOF retains its crystallinity and porosity even after th

59 n characteristics, construction of composite MOFs and amorphous MOFs, as well as providing new synthe

60 e dispersed Zr sites present in the confined MOF, and the loading of the mesoporous SiO2 , is demonst

61 the design and synthesis of highly connected MOFs based on reticulation of the sole two edge-transiti

62 hat, unlike other dithienylethene-containing MOFs, the properties of the pore can be changed via an o

63 that previously measured in its conventional MOF counterparts.

64 ies the structural diversity of conventional MOFs can also be applied to the self-assembly of protein

65 to characteristics of edge-transitive {Cu2} MOFs with A3X4 stoichiometry.

66 mechanically robust conformed and densified MOFs for high volumetric energy storage and other indust

67 Thus, we survey dye@MOF composites as novel media in which efficient upconve

68 onditions to synthesize readily exfoliatable MOF nanosheets, functionalized in situ by adopting the g

69 c avenue to enlarge the limited number of FE MOFs.

70 h yielded an expanded library of 15 ferritin-MOFs with the expected body-centered (cubic or tetragona

71 attice symmetries and dimensions of ferritin-MOFs can be dictated by both the metal and linker compon

72 tablishes that the self-assembly of ferritin-MOFs is highly robust and that the synthetic modularity

73 rystalline samples reveal that some ferritin-MOFs can adopt multiple lattice conformations, suggestin

74 rthermore, the bromine pre-adsorbed flexible MOFs can be used as generic bromine sources for brominat

75 A series of flexible MOFs (PCN-605, PCN-606, and PCN-700) are synthesized and

76 The flexible MOFs act as bromine-nanocontainers which elongate the st

77 3.02; P < .05), and benzodiazepines (aHR for MOF, 1.15; 95% CI, 1.04-1.26; P < .05; aHR for hip fract

78 1.18-1.85; P < .05), antipsychotics (aHR for MOF, 1.43; 95% CI, 1.15-1.77; P < .05; aHR for hip fract

79 ctive serotonin reuptake inhibitors (aHR for MOF, 1.43; 95% CI, 1.27-1.60; P < .05; aHR for hip fract

80 ortunities and challenges are identified for MOF-enabled device functionality and technological appli

81 hese are the highest values yet observed for MOF solid electrolytes.

82 s well as providing new synthetic routes for MOF preparation.

83 -balancing Li(+), Na(+), and Mg(2+) ions for MOFs.

84 r, which is amongst the highest reported for MOFs under these conditions and is much higher than the

85 fraction measurements indicate that all four MOFs adsorb DMMP (introduced at atmospheric pressures th

86 t nontraumatic major osteoporotic fractures (MOFs) and hip fractures.

87 e critical steps in metal-organic framework (MOF) activation involving solvent exchange and solvent e

88 ered nanopores of a metal-organic framework (MOF) are exploited to encapsulate and homogeneously disp

89 a chiral Cu(II) 3D metal-organic framework (MOF) based on the tripeptide Gly-l-His-Gly (GHG) for the

90 acid (BODCA)-MOF, a metal-organic framework (MOF) built with a high-symmetry bicyclo[2.2.2]octane dic

91 recently developed metal-organic framework (MOF) catalyst for the dimerization of ethylene has a com

92 bility underpinning metal-organic framework (MOF) confers a versatile platform to contrive next-gener

93 The aluminum-based metal-organic framework (MOF) made from 2-aminoterephthalate is a photocatalyst f

94 on the nodes of the metal-organic framework (MOF) NU-1000 are active for oxidation of methane to meth

95 Kr, and Xe) on the metal-organic framework (MOF) NU-1000, which is one of the most thermally stable

96 A major goal of metal-organic framework (MOF) research is the expansion of pore size and volume.

97 in a robust azolate metal-organic framework (MOF) to produce stable and safe-to-handle Co(III) materi

98 ovel Cu(II)-azolate metal-organic framework (MOF) with tubular pores undergoes a reversible single cr

99 e-functionalized Zr metal-organic framework (MOF), UiO-66-NH2 (Pt@UiO-66-NH2 ) as a multifunctional c

100 ed rare-earth-based metal-organic framework (MOF), with dual functionality for moisture control withi

101 a robust and porous metal-organic framework (MOF), Zr12-TPDC, constructed from triphenyldicarboxylic

102 microstructure of metal-organic frameworks (MOFs) after postsynthetic exchange (PSE) reveals that th

103 are a subclass of metal-organic frameworks (MOFs) amenable to significant property tuning by alterin

104 , the potential of metal-organic frameworks (MOFs) and covalent organic frameworks (COFs) as platform

105 Metal-organic frameworks (MOFs) are a class of modular, crystalline, and porous ma

106 Metal-organic frameworks (MOFs) are crystalline porous materials with designable t

107 cs, titanium based metal-organic frameworks (MOFs) are one of the most appealing classes of MOFs repo

108 l applications for metal organic frameworks (MOFs) are tantalizing.

109 Porous metal-organic frameworks (MOFs) are the subject of considerable research interest

110 Metal-organic frameworks (MOFs) are typically highlighted for their potential appl

111 Utilizing metal-organic frameworks (MOFs) as a biological carrier can lower the amount of th

112 The influence of metal-organic frameworks (MOFs) as additives is herein described for the reaction

113 cal feasibility of metal-organic frameworks (MOFs) as novel delivery systems for encapsulation and co

114 niversity of Oslo) metal-organic frameworks (MOFs) can be transformed into self-propelled micromotors

115 able properties of metal-organic frameworks (MOFs) can be tuned by chemical functionalization of the

116 Metal-organic frameworks (MOFs) define emerging materials with unique optoelectron

117 ification (PSM) of metal-organic frameworks (MOFs) has attracted much attention due to the possibilit

118 urface tunability, Metal-Organic Frameworks (MOFs) have been gaining popularity as candidates for enz

119 cles (MNPs) within metal-organic frameworks (MOFs) have broad applications in many fields.

120 Metal-organic frameworks (MOFs) have emerged as an exciting class of porous materi

121 Metal-organic frameworks (MOFs) have potential applications as energy absorbing ma

122 Metal-organic frameworks (MOFs) have rapidly grown into a major area of chemical r

123 Metal-organic frameworks (MOFs) have shown promising behavior for adsorption cooli

124 o-dimensional (2D) metal-organic frameworks (MOFs) into fabrics through direct solution-phase self-as

125 rol of porosity of metal-organic frameworks (MOFs) is of critical importance to their materials funct

126 compounds, called metal-organic frameworks (MOFs) or coordination polymers, has been investigated in

127 Metal-organic frameworks (MOFs) or porous coordination polymers (PCPs) are open, c

128 polymers (CPs) and metal-organic frameworks (MOFs) results not only in a plethora of materials that c

129 or applications of metal-organic frameworks (MOFs) such as gas storage and separation, flexibility is

130 n this manuscript, metal-organic frameworks (MOFs) were investigated as a model system for engineerin

131 locks for creating metal-organic frameworks (MOFs) with controllable topologies.

132 is the subclass of metal-organic frameworks (MOFs) with pore aperture sizes below 5-7 A, namely ultra

133 Two porous, chiral metal-organic frameworks (MOFs), Ca14(l-lactate)20(acetate)8(C2H5OH)(H2O) (MOF-120

134 Metal-organic frameworks (MOFs), with their well-ordered pore networks and tunable

135 (metallo)porphyrin metal-organic frameworks (MOFs), ZrPP-n (n = 1, 2), featuring infinite Zr(IV) -oxo

136 aviour of flexible metal-organic frameworks (MOFs)-porous crystalline materials that undergo a struct

137 evement for porous metal-organic frameworks (MOFs).

138 rodes in EDLCs, is metal-organic frameworks (MOFs).

139 nd construction of metal-organic frameworks (MOFs).

140 ., true polymorph) metal-organic frameworks (MOFs).

141 ctricity in chiral metal-organic frameworks (MOFs): following a single-crystal to single-crystal cati

142 y exhibit effective selectivity derived from MOF cavities, but also enhanced catalytic activity due t

143 ged as a versatile approach to functionalize MOF surfaces with a wide variety of catalytic metal-oxo

144 NU-1000 provide an active, first generation MOF-based, selective methane oxidation catalyst.

145 linkers presented by the topology of a given MOF that are primed to form such an excited state comple

146 Gram for gram, MOFs can absorb as much energy as a high explosive can r

147 d MNPs and as a sacrificial template to grow MOFs.

148 chemical sensing opened up by the new guest@MOF composite systems is shown.

149 functionalized in situ by adopting the guest@MOF (host) strategy, is developed.

150 OF-1201) and Ca6(l-lactate)3(acetate)9(H2O) (MOF-1203), are constructed from Ca(2+) ions and l-lactat

151 ), Ca14(l-lactate)20(acetate)8(C2H5OH)(H2O) (MOF-1201) and Ca6(l-lactate)3(acetate)9(H2O) (MOF-1203),

152 of a series of 14 interpenetrated Zr and Hf MOFs linked by functionalized 4,4'-[1,4-phenylene-bis(et

153 A new hierarchical MOF consisting of Cu(II) centers connected by benzene-tr

154 A soft porous Zn(II)-MOF (1) displays distinctive three-step hysteretic breat

155 n control of the chemistry of CO2 capture in MOF materials and one that highlights the importance of

156 The difference in MOF nucleation and growth kinetics of the two solutions

157 Notably, atomic layer deposition (ALD) in MOFs has recently emerged as a versatile approach to fun

158 The uniform catalytic sites available in MOFs provide a unique opportunity to directly study reac

159 he release of AITC molecules encapsulated in MOFs.

160 hese studies demonstrate that metal nodes in MOFs mimic homogeneous catalysts not just functionally,

161 dsorption isotherms of fluorocarbon R134a in MOFs.

162 servation, 5750 (8.4%) sustained an incident MOF, 1579 (2.3%) sustained an incident hip fracture, and

163 es of framework reorganization in individual MOF nanocrystals is largely unknown.

164 easure the mechanical behavior of individual MOF nanocrystals under compression within a transmission

165 gy that enables MNPs to be encapsulated into MOFs with controllable spatial localization by using met

166 torage performance of a family of isomorphic MOFs based upon PCN-14.

167 ocalization of bdc-NH2 in these mixed-linker MOFs.

168 cal developments in the field of luminescent MOF and MOF-based photonic crystals/thin film sensory ma

169 moderate solvothermal conditions could make MOFs an exceptionally powerful tool to address fundament

170 performing material previously reported, Mg-MOF-74.

171 the latest developments in ultra-microporous MOF adsorbents and their use as separating agents via th

172 Microporous MOFs with robust metal nodes and pro-labile linkers were

173 sizes below 5-7 A, namely ultra-microporous MOFs, which in contrast to conventional zeolites and act

174 r to the surface of MOFs, the resultant MNPs@MOF composites not only exhibit effective selectivity de

175 Nanoindentation tests on the monolithic MOF showed robust mechanical properties, with hardness a

176 of a supercapacitor made entirely from neat MOFs as active materials, without conductive additives o

177 n, these issues must be addressed when a new MOF structure is determined and reported.

178 ylene rings, we construct moisture-stable Ni-MOF-74 members with adjustable pore apertures, which exh

179 ighlights the opportunity in designing novel MOF-supported single-site solid catalysts by tuning the

180 It is challenging to observe MOFs with transmission electron microscopy (TEM) due to

181 s identify the first experimentally observed MOF that exhibits band-like metallic conductivity.

182 for a series of isoreticular octacarboxylate MOFs, denoted MFM-180 to MFM-185, via a strategy of sele

183 al conditions were as follows: the amount of MOF-545, 10mg; pH of sample, 7; adsorption and elution t

184 The applications of MOF-enzyme composites, primarily in transferation, catal

185 The surface area of MOF-545 was found to be 2192m(2)/g.

186 Furthermore, new classes of MOF sensory materials utilizing advanced signal transduc

187 his review summarizes recent developments of MOF-enzyme composites with special emphasis on preparati

188 However, the function of MOF in hematopoietic stem cell (HSC) development has not

189 lating the external surface functionality of MOF nanoparticles are less developed.

190 The hydrolysis of MOF-1201 in water makes it the first example of a degrad

191 ain its position as the definitive method of MOF structure determination, these issues must be addres

192 er-resolution microscopy reveals movement of MOF particles when located outside of the cell boundary,

193 ments with catalytically inactive mutants of MOF showed that its enzymatic activity was required to m

194 implanted into the coordination nanospace of MOF materials.

195 tionalization of the external metal nodes of MOF nanoparticles with terminal phosphate-modified oligo

196 It also underestimated the 10-year risk of MOF by 36% for use of selective serotonin reuptake inhib

197 s is attributed to the chemical stability of MOF in low pH environment and to the protease resistance

198 Lastly we present the current state of MOF commercialization with direct feedback from commerci

199 As the subfield of MOF-based sensing has developed, many diverse chemical f

200 nits can be anchored on the outer surface of MOF NPs in a self-assembly process generating multifunct

201 esult, we demonstrated that the tailoring of MOF electronic properties could be performed as a functi

202 Successful utilization of MOF modularity also allowed us to structurally character

203 ts herein aid in the efficient activation of MOFs in both laboratory and industrial settings and prov

204 sing the myriad of potential applications of MOFs by enabling larger scale production and hence real-

205 terest in and many potential applications of MOFs, such as in gas storage, catalysis, sensing and dru

206 ecifically we bring together many aspects of MOFs that underpin their stability, reactivity and dynam

207 is review we concentrate on the chemistry of MOFs.

208 Fs) are one of the most appealing classes of MOFs reported to date.

209 ll critically depend on the compatibility of MOFs with existing fabrication protocols and predominant

210 ity and endothermicity during deformation of MOFs shows a surprising potential for absorption and dis

211 copy (TEM) due to the extreme instability of MOFs upon electron beam irradiation.

212 to be overcome to enable the integration of MOFs with technologies where these promising traits can

213 est molecules to improve the performances of MOFs in adsorption and catalysis.

214 mediating role of water within the pores of MOFs.

215 The high porosity of MOFs, however, is conventionally coupled to very poor el

216 Finally, we discuss the potential of MOFs as materials in which several single-site catalytic

217 Experimental prescreening of MOFs was performed based on changes in the density of el

218 In the presence of MOFs with UMCM-1 and MOF-5 topologies, the reaction is s

219 play an important role in the properties of MOFs and can significantly change the pore architecture.

220 standing of the distinguishing properties of MOFs and eliminating fabrication-related obstacles for i

221 or transforming the electronic properties of MOFs from insulating to semiconducting, as well as provi

222 ns we also target the photonic properties of MOFs that benefit from their porosity, and resulting fro

223 key role in the photophysical properties of MOFs.

224 e of the most common reactions in the PSM of MOFs.

225 Recently, a selection of MOFs has been demonstrated to undergo melting and vitrif

226 ptical band gap, varies across the series of MOFs and is a function of the relative orientation of th

227 framework topology give rise to a series of MOFs with a remarkable range of physical properties that

228 e encapsulated MNPs closer to the surface of MOFs, the resultant MNPs@MOF composites not only exhibit

229 organic molecules or on the pore surfaces of MOFs, in a very fast (1-2 s) and continuous way.

230 the inherent structural features/topology of MOFs and the associated gas/vapour separation performanc

231 d structural and compositional tunability of MOFs, these results herald the advent of a new generatio

232 way significantly reduced cellular uptake of MOFs.

233 This is the first study of the use of MOFs for biofouling control in membranes.

234 nced signal transduction by devices based on MOF photonic crystals and thin films have been developed

235 constants, are also found to be dependent on MOF identity.

236 hese are the unusual examples of Zr-MOFs (or MOFs in general) based on phenolic porphyrins, instead o

237 d conditions, suggesting that defect-ordered MOFs could be a productive route to porous two-dimension

238 Thermal treatment of the oxidized MOF causes homolytic cleavage of the Co(III)-halogen bon

239 ne zirconium phosphonate and the only porous MOF material reported to survive in aqua regia.

240 ough design of organic linkers within porous MOF materials.

241 c aspects of substrate binding within porous MOFs.

242 Taking the high number of possible MOF NPs and different functional units into account, the

243 e DNA damage, offering a rationale to pursue MOF inhibitors as a targeted approach to treat MLL-rearr

244 This is the first time that RE-MOFs based on 12-c molecular building blocks (MBBs), d6R

245 ient HER catalytic properties among reported MOFs.

246 applied to the design of stimuli-responsive MOFs.

247 ation to the amino groups, and the resulting MOF is an efficient photocatalyst for overall water spli

248 upported on the external surface of the same MOF (Pt/UiO-66-NH2 ).

249 E as a method for the creation of core-shell MOFs.

250 e captured high-resolution 3D images showing MOF uptake by HeLa cells over a 24 h period.

251 re building unit, affording the first Cu-shp-MOF.

252 led to the formation of the targeted RE-shp-MOF.

253 Y-shp-MOF-5 exhibits exceptional structural integrity, robustn

254 Here we report Y-shp-MOF-5, a hybrid microporous highly connected rare-earth-

255 ble hierarchical porous structures in stable MOFs, which facilitates the diffusion and adsorption pro

256 0, which is one of the most thermally stable MOFs.

257 ting point for further selection of suitable MOFs.

258 ability of a Cu-azobenzene tetracarboxylate MOF (JUC-62) for low-energy CO2 capture.

259 The discovery that MOF and its H4K16ac activity are required for adult but

260 These results demonstrate that MOFs can be powered by various engines and halted by dif

261 Endocytosis analysis revealed that MOFs are internalized by active transport and that inhib

262 The MOF becomes amorphous in >60% relative humidity; however

263 The MOF construct containing 60% PTA by weight produces isoa

264 Additionally, the MOF nanocrystals provided biocidal activity that lasted

265 rovided by the protective cage formed by the MOF around the encapsulated enzymes.

266 ucture of metal-oxo species deposited in the MOF NU-1000 through ALD.

267 ntradicts any notion that degradation of the MOF at grain boundaries is enabling the observed conduct

268 Desolvation of the MOF in two different solvents leads to two polymorphic a

269 strates that amination of all linkers of the MOF is not required to obtain the maximum photocatalytic

270 al isotherms indicate similar filling of the MOF surface by the different gases, starting with strong

271 t, further demonstrating the capacity of the MOF to contain a high concentration of active sites nece

272 es positioned on the external surface of the MOF, the construct shows a high catalytic activity for h

273 gulation of MNPs as close as possible to the MOF surface.

274 species and how they are tethered within the MOF is critical to understanding how these components co

275 fication at the amino group sites within the MOF.

276 These MOFs exhibit similar pore size, pore surface, and surfac

277 the release of AITC molecules from all these MOFs was triggered under high RH (95-100%) conditions.

278 /g) are absorbed by the compression of these MOFs.

279 and GC headspace analyses showed that these MOFs could encapsulate and retain AITC molecules within

280 d NU-901, while taking care to utilize these MOFs' large pore volume and size to achieve exceptional

281 This MOF can be modified by incorporating Ni(2+) cations into

282 The linkers in this MOF are pyrenes linked to the nodes via the carboxylate

283 view the fundamentals of adsorption in this MOF series.

284 We illustrate the application of this MOF to chemical separations.

285 Though MOFs have been studied in bulk forms, ways of deliberate

286 Not only Ti-MOFs but also Ti-oxo-clusters will be discussed and part

287 roadmap to stimulate the next steps towards MOF-based microelectronics within the community.

288 Using spray drying, we show the PSM of two MOFs, the amine-terminated UiO-66-NH2 and the aldehyde-t

289 nickel isonicotinate based ultramicroporous MOF, 1 [Ni-(4PyC)2.DMF], that has the lowest PE for post

290 terials through utilization of unprecedented MOF modularity, which cannot be replicated in any other

291 n applications, but also for instances where MOFs serve as components of functional nanodevices.

292 r FRAX score, depression was associated with MOF (adjusted hazard ratio [aHR], 1.39; 95% CI, 1.27-1.5

293 e and fabrication of electronic devices with MOF-based components has not been widely explored, despi

294 tion of light and afford photocatalysis with MOFs under visible-light irradiation.

295 the limitation of molecular diffusion within MOF channels.

296 lled spatial distribution of the MNPs within MOFs remains a challenge for addressing key issues in ca

297 Mx-yM'y-MOFs, MxM'y-MOFs, and Mx(ligand-M'y)-MOFs, in which the second metal (M') incorporation occur

298 s of bimetallic systems, Mx-yM'y-MOFs, MxM'y-MOFs, and Mx(ligand-M'y)-MOFs, in which the second metal

299 tinct classes of bimetallic systems, Mx-yM'y-MOFs, MxM'y-MOFs, and Mx(ligand-M'y)-MOFs, in which the

300 These are the unusual examples of Zr-MOFs (or MOFs in general) based on phenolic porphyrins,