laboratory equipment and services Environment and Pollution

Catalytic Light Induced Tender

πŸ›οΈ TECHNISCHE UNIVERSITAET MUENCHEN GERMANY
πŸ“„ Tender ID: 503464960 πŸ“… Published: 02 May 2024

πŸ“‹ Tender Overview

Catalytic Light-Induced Deracemization
Molecules Are Chiral If They Exist In Two Forms, Called Enantiomers, Which Behave Like Image And Mirror Image. In Many Applications, E.G. In Medicine, Nutrition, And Crop Protection, Chiral Molecules Are Required As A Single Enantiomer (Enantiomerically Pure Compound) But Not As A Mixture (Racemate). The Market For Enantiomerically Pure Compounds Exceeds 100 Billion € Annually And Continues To Grow Rapidly. Despite Significant Recent Advances In Asymmetric Catalysis, Many Chiral Compounds Are For Cost Reasons Prepared As Racemates And Separated Thereafter. If Only One Enantiomer Is Required, The Other Enantiomer Remains As Waste. The Aim Of The Calide Project Is To Provide For The First Time A Comprehensive Set Of Methods For The Quantitative Conversion Of Racemates Into Single Enantiomers Employing Exclusively Light And A Photocatalyst. The Process Includes The Light-Induced Formation Of Short-Lived Achiral Intermediates Which Decay To The Starting Materials On A Thermal Reaction Channel. By Employing Two Intrinsically Different Channels For Formation And Decay, The Transformation Overcomes Issues Of Microscopic Reversibility Which Render Related Thermal Deracemization Reactions Impossible. The Photocatalyst Interacts With The Racemic Substrates And Enables The Destruction And Reformation Of The Stereogenic Element. A First Objective (Work Package I) Is To Identify Suitable Binding Motifs To Achieve The Required Proximity In The Energy Transfer Step For Compounds Displaying An Axis Or Plane Of Chirality. The Second Objective (Work Package Ii) Aims At A Deracemization Of Compounds With A Stereogenic Carbon Center Via A Reversible Cleavage Of Carbon-Carbon Or Carbon-Heteroatom Bonds. The Bond Cleavage Can Be Initiated By Energy Or Electron Transfer. The Third Objective (Work Package Iii) Tackles Substrates With A Carbon-Hydrogen Bond At The Stereogenic Carbon Atom. Bond Fission By Hydrogen Abstraction From The Catalyst Is Proposed As The Key Feature Of This Method.
Funded Under
European Research Council (Erc)
Total Cost
€ 2 447 299,00
Eu Contribution
€ 2 447 299,00
Coordinated By
Technische Universitaet Muenchen
Germany
Start Date
1 January 2025
End Date
31 December 2029

Objective

Molecules are chiral if they exist in two forms, called enantiomers, which behave like image and mirror image. In many applications, e.g. in medicine, nutrition, and crop protection, chiral molecules are required as a single enantiomer (enantiomerically pure compound) but not as a mixture (racemate). The market for enantiomerically pure compounds exceeds 100 billion € annually and continues to grow rapidly. Despite significant recent advances in asymmetric catalysis, many chiral compounds are for cost reasons prepared as racemates and separated thereafter. If only one enantiomer is required, the other enantiomer remains as waste. The aim of the CALIDE project is to provide for the first time a comprehensive set o

πŸ” Key Information

πŸ“„
Tender Reference No.
503464960
πŸ“…
Publication Date
02 May 2024
πŸ’°
Estimated Value
N/A
🌐
Sector
laboratory equipment and services
πŸ“…
Deadline
31 Dec 2029
πŸ“
Notice Type
Projects
πŸ“
Location
Sweden
πŸ“‘
Contract Duration
5 Years 7 Months 29 Days

πŸ“ Documents & Downloads

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🧭 Quick Facts

Authority TECHNISCHE UNIVERSITAET MUENCHEN GERMANY
Country Sweden
State / UT N/A
Tender Type Project Information
Currency SEK
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