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Dive into the research topics where Maryam Shafaei-Fallah is active.

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Featured researches published by Maryam Shafaei-Fallah.


Journal of the American Chemical Society | 2011

Ion-Exchangeable Cobalt Polysulfide Chalcogel

Maryam Shafaei-Fallah; Jiaqing He; Alexander Rothenberger; Mercouri G. Kanatzidis

We present a promising approach in synthetic chalcogel chemistry that is extendable to a broad variety of inorganic spacers. Polychalcogenide aerogels with ion-exchange properties are demonstrated in cobalt polysulfide. The new materials show a broad range of pore sizes and high surface area of 483 m(2)/g.


Advanced Materials | 2011

Extraordinary Selectivity of CoMo3S13 Chalcogel for C2H6 and CO2 Adsorption

Maryam Shafaei-Fallah; Alexander Rothenberger; Alexandros P. Katsoulidis; Jiaqing He; Christos D. Malliakas; Mercouri G. Kanatzidis

or metals, [ 5 ] has recently been expanded to include the emerging new chalcogenide materials called chalcogels. [ 6–10 ] Unlike the nanocrystalline chalcogenide aerogels reported by Brock et al., [ 6 , 11 , 12 ] the chalcogels feature random amorphous networks similar to those of silica. Because of the “soft” nature of electron-rich chalcogen atoms, the polarizability of the internal surface of chalcogels is much higher than those of metal oxides, porous carbons, and organic polymers and therefore provides an entirely new medium through which to study the diffusion and separation of gases. [ 13 ] Photocatalysis, catalysis, gas separation, and removal of heavy metals with chalcogels are just some of the proposed applications that make use of the unique electronic properties (tunable bandgaps and high surface polarizability) of such high surface area materials. [ 8 ]


Inorganic Chemistry | 2010

Aluminosilicate Relatives: Chalcogenoaluminogermanates Rb3(AlQ2)3(GeQ2)7 (Q = S, Se)

Alexander Rothenberger; Maryam Shafaei-Fallah; Mercouri G. Kanatzidis

The new compounds Rb(3)(AlQ(2))(3)(GeQ(2))(7) [Q = S (1), Se (2)] feature the 3D anionic open framework [(AlQ(2))(3)(GeQ(2))(7)](3-) in which aluminum and germanium share tetrahedral coordination sites. Rb ions are located in channels formed by the connection of 8, 10, and 16 (Ge/Al)S(4) tetrahedra. The isostructural sulfur and selenium derivatives crystallize in the space group P2(1)/c. 1: a = 6.7537(3) Å, b = 37.7825(19) Å, c = 6.7515(3) Å, and β = 90.655(4)°. 2: a = 7.0580(5) Å, b = 39.419(2) Å, c = 7.0412(4) Å, β = 90.360(5)°, and Z = 2 at 190(2) K. The band gaps of the congruently melting chalcogenogermanates are 3.1 eV (1) and 2.4 eV (2).


Chemical Communications | 2007

A recipe for new organometallic polymers and oligomers? Synthesis and structure of an oligo- and a polymeric arrangement of P–S anions

Alexander Rothenberger; Maryam Shafaei-Fallah; Weifeng Shi

A route to organometallic polymers and oligomers is described using metal complexes with P/S-ligands as examples.


Dalton Transactions | 2006

Metal thiophosphonates and related compounds : an emerging area of supramolecular coordination chemistry

Weifeng Shi; Maryam Shafaei-Fallah; Christopher E. Anson; Alexander Rothenberger

Nine new compounds containing PS ligands of the types [P(OtBu)S3]2-, [ArP(StBu)S2]- and [ArP(OtBu)S2]- are reported (Ar = 4-anisyl). It is demonstrated that the topology of alkali metal ion and ligand composition influence the structure of supramolecular arrangements.


Dalton Transactions | 2005

Functionalised trimethylsilyl reagents in cluster synthesis: reactions of Ph2P(S)SSiMe3 with group 11 salts

Maryam Shafaei-Fallah; Christopher E. Anson; Dieter Fenske; Alexander Rothenberger

A series of complexes, ranging from the small cluster 1/infinity[Ag(Ph2PS2)(dppe)](infinity) [dppe=1,2-bis(diphenylphosphino)ethane] to [Cu48S20(O(t)Bu)2(Ph2PS2)2(dppm-)4(dppm)4][dppm=1,2-bis(diphenylphosphino)methane] (the largest Cu cluster containing phosphinodithioato ligands), has been synthesised. The structural evidence presented here indicates that in these reactions initially small cyclic aggregates or one-dimensional coordination polymers are formed. The growth of these intermediates to larger aggregates can take up to several months and could proceed via cationic intermediates.


Advanced Materials | 2011

Extraordinary selectivity of CoMo 3 S 13 chalcogel for C 2 H 6 and CO 2 adsorption

Maryam Shafaei-Fallah; Alexander Rothenberger; Alexandros P. Katsoulidis; Jiaqing He; Christos D. Malliakas; Mercouri G. Kanatzidis

or metals, [ 5 ] has recently been expanded to include the emerging new chalcogenide materials called chalcogels. [ 6–10 ] Unlike the nanocrystalline chalcogenide aerogels reported by Brock et al., [ 6 , 11 , 12 ] the chalcogels feature random amorphous networks similar to those of silica. Because of the “soft” nature of electron-rich chalcogen atoms, the polarizability of the internal surface of chalcogels is much higher than those of metal oxides, porous carbons, and organic polymers and therefore provides an entirely new medium through which to study the diffusion and separation of gases. [ 13 ] Photocatalysis, catalysis, gas separation, and removal of heavy metals with chalcogels are just some of the proposed applications that make use of the unique electronic properties (tunable bandgaps and high surface polarizability) of such high surface area materials. [ 8 ]


Advanced Materials | 2012

Extraordinary Selectivity of CoMo[subscript 3]S[subscript 13] Chalcogel for C[subscript 2]H[subscript 6] and CO[subscript 2] Adsorption

Maryam Shafaei-Fallah; Alexander Rothenberger; Alexandros P. Katsoulidis; Jiaqing He; Christos D. Malliakas; Mercouri G. Kanatzidis

or metals, [ 5 ] has recently been expanded to include the emerging new chalcogenide materials called chalcogels. [ 6–10 ] Unlike the nanocrystalline chalcogenide aerogels reported by Brock et al., [ 6 , 11 , 12 ] the chalcogels feature random amorphous networks similar to those of silica. Because of the “soft” nature of electron-rich chalcogen atoms, the polarizability of the internal surface of chalcogels is much higher than those of metal oxides, porous carbons, and organic polymers and therefore provides an entirely new medium through which to study the diffusion and separation of gases. [ 13 ] Photocatalysis, catalysis, gas separation, and removal of heavy metals with chalcogels are just some of the proposed applications that make use of the unique electronic properties (tunable bandgaps and high surface polarizability) of such high surface area materials. [ 8 ]


Advanced Materials | 2011

Extraordinary Selectivity of CoMo3S13Chalcogel for C2H6and CO2Adsorption

Maryam Shafaei-Fallah; Alexander Rothenberger; Alexandros P. Katsoulidis; Jiaqing He; Christos D. Malliakas; Mercouri G. Kanatzidis

or metals, [ 5 ] has recently been expanded to include the emerging new chalcogenide materials called chalcogels. [ 6–10 ] Unlike the nanocrystalline chalcogenide aerogels reported by Brock et al., [ 6 , 11 , 12 ] the chalcogels feature random amorphous networks similar to those of silica. Because of the “soft” nature of electron-rich chalcogen atoms, the polarizability of the internal surface of chalcogels is much higher than those of metal oxides, porous carbons, and organic polymers and therefore provides an entirely new medium through which to study the diffusion and separation of gases. [ 13 ] Photocatalysis, catalysis, gas separation, and removal of heavy metals with chalcogels are just some of the proposed applications that make use of the unique electronic properties (tunable bandgaps and high surface polarizability) of such high surface area materials. [ 8 ]


Chemistry: A European Journal | 2007

Polymeric organometallic architectures of novel P-Se anions.

Weifeng Shi; Maryam Shafaei-Fallah; Le Zhang; Christopher E. Anson; Eberhard Matern; Alexander Rothenberger

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Alexander Rothenberger

King Abdullah University of Science and Technology

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Weifeng Shi

Karlsruhe Institute of Technology

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Christopher E. Anson

Karlsruhe Institute of Technology

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Jiaqing He

University of Science and Technology

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Le Zhang

Karlsruhe Institute of Technology

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Dieter Fenske

Karlsruhe Institute of Technology

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Claudia Schrodt

Karlsruhe Institute of Technology

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