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, long before the emergence of life. The central aim is to understand how simple organic compounds, produced under plausible prebiotic conditions, could polymerize into organofilms, influence carbonate
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enables high activity in olefin polymerization, while providing precise control over composition and molecular weight distribution. However, this activator remains a poorly defined solid at the structural
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different polymerization processes, e.g. free radical and cationic polymerization. In this configuration you can cure two different polymers in principle independently and generate spacial property variation
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to the polymers, and complexing units to allow the polymers to interact with metal ions [1]. The target polymers will be synthesized by controlled radical polymerization or telomerization. The proposed method is
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: Impact of metal or metal alloy crystallographic orientation on ammonia electrocatalysis to enable design of the most efficient catalysts. Understanding what controls electrocatalytic stability, long term
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, including drug delivery, tissue regeneration, and wound healing. However, the use of polymeric materials for wound healing applications is severely limited by their inefficacy to induce a biological response
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applications in programmable matter and morphing structures. While considerable progress has been made in controlling both the spatial and temporal dimensions of matter, the crucial step is translating
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are revolutionising the field of tissue engineering and regenerative medicine by enabling precise spatial control over the composition, architecture, and bioactivity of printed constructs. Within this transformative