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Metal-organic networks

The structural richness and diversity of the metal-organic networks obtained by reaction of Cul and CuBr with ArSC4SAr (C4 = (CH2)4, CH2C=CCH2) are summarized in Scheme 10. [Pg.125]

Catalysis by metal-organic solids may also be applied to redox reactions. An especially intriguing target would be manipulation of hydrocarbon transformations. Many metal-organic networks so far reported in fact contain redox-active transition metals (Cu , Pd", Co" and so on). Metalloporphyrins are potential... [Pg.158]

Scheme 4 illustrates some of the 2-D network motifs that have thus far been observed in coordination polymers. Square-grid networks (Scheme 4a) exemplify a particularly simple and commonly reported example of a predictable 2-D metal-organic network. Square-grid coordination polymers are based upon 1 2 metahligand complexes with linear bifunctional linkers. Grids with two tjmes of linkers have also been reported, in which rectangular grids are formed (Scheme 4c). ... [Pg.244]

Conformational flexibility in ligands can lead to conformational snpramolecular isomers in metal-organic network systems. For example, hydrothermal crystallization using an aminotriazole ligand afforded two 3D supramolecular... [Pg.2437]

Mmguez Espallargas G, Brammer L, Allan DR, Pulham CR, Robertson N, Warren JE (2008) Noncovalent interactions under extreme conditions high-pressure and low-temperature diffi-action studies of the isostructural metal-organic networks (4-chloropyridinium)2[CoX4] (X=C1, Br). J Am Chem Soc 130 9058-9071... [Pg.110]

Scheme 5 The HTT molecule (14), together with two other rigid, trigonal molecules (15 and 16), for directly reacting with metal species (e.g., PtClj for 15 and BiClj for 16) to produce covalent metal-organic networks with porous and semiconductive properties... Scheme 5 The HTT molecule (14), together with two other rigid, trigonal molecules (15 and 16), for directly reacting with metal species (e.g., PtClj for 15 and BiClj for 16) to produce covalent metal-organic networks with porous and semiconductive properties...
BET = Brunauer-Emmett-Teller CMON = covalent metal-organic networks CTF = covalent triazine-based framework DCQNI = A,A -dicyanoquinodiimine DEF = A,A-diethylformamide DMA = A,A-dimethyl-acetamide FP-TRMC = flash-photolysis time-resolved microwave conductivity HHT = 2,3,6,7,10,11-hexa-hydroxytriphenylene M-CAT = metal-catecholate PSM = postsynthesis modifications PXRD = powder X-ray diffraction TCNQ = tetracyanoquinodimethane TOF = time-of-flight TTF = tetrathiafulvalene. [Pg.383]

CMON covalent metal-organic networks EXAFS... [Pg.565]


See other pages where Metal-organic networks is mentioned: [Pg.152]    [Pg.236]    [Pg.246]    [Pg.263]    [Pg.264]    [Pg.270]    [Pg.70]    [Pg.23]    [Pg.24]    [Pg.25]    [Pg.78]    [Pg.157]    [Pg.791]    [Pg.997]    [Pg.1003]    [Pg.312]    [Pg.86]    [Pg.66]    [Pg.380]    [Pg.288]    [Pg.192]   
See also in sourсe #XX -- [ Pg.125 , Pg.152 ]




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Metal-organic coordination networks

Metal-organic frameworks (MOFs network topologies

Network Organic

Organization network

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