Ahibur Rahaman (Former)
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- 2023
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Mark
Synthesis of phosphine derivatives of [Fe2(CO)6(μ-sdt)] (sdt = SCH2SCH2S) and investigation of their proton reduction capabilities
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- Contribution to journal › Article
- 2021
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Mark
Sequential infiltration synthesis and pattern transfer using 6 nm half-pitch carbohydrate-based fingerprint block copolymer
2021) Advances in Patterning Materials and Processes XXXVIII 2020 In Proceedings of SPIE - The International Society for Optical Engineering 11612.(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
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Mark
Proton reduction by phosphinidene-capped triiron clusters
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- Contribution to journal › Article
- 2020
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Mark
Photoexcitation dynamics in electrochemically charged CdSe quantum dots : From hot carrier cooling to auger recombination of negative trions
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- Contribution to journal › Article
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Mark
Asymmetric hydrogenation of an α-unsaturated carboxylic acid catalyzed by intact chiral transition metal carbonyl clusters-diastereomeric control of enantioselectivity
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- Contribution to journal › Article
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Mark
Electrocatalytic proton-reduction behaviour of telluride-capped triiron clusters : tuning of overpotentials and stabilization of redox states relative to lighter chalcogenide analogues
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- Contribution to journal › Article
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Mark
Electron Transfer Mediated by Iron Carbonyl Clusters Enhance Light-Driven Hydrogen Evolution in Water by Quantum Dots
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- Contribution to journal › Article
- 2019
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Mark
Chalcogenide-capped triiron clusters [Fe3(CO)9(μ3-E)2], [Fe3(CO)7(μ3-CO)(μ3-E)(μ-dppm)] and [Fe3(CO)7(μ3-E)2(μ-dppm)] (E = S, Se) as proton-reduction catalysts
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- Contribution to journal › Article
- 2018
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Mark
Synthesis and molecular structures of the 52-electron triiron telluride clusters [Fe3(CO)8(μ3-Te)2(κ2-diphosphine)] - Electrochemical properties and activity as proton reduction catalysts
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- Contribution to journal › Article
- 2017
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Mark
Synthesis and characterization of chiral phosphirane derivatives of [(μ-H)4Ru4(CO)12] and their application in the hydrogenation of an α,β-unsaturated carboxylic acid
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- Contribution to journal › Article