Articles posted by: admin

Introduction

N,N-Bis(2-dimethylaminoethyl) ether (BDMAEE) has garnered attention in the field of transition metal catalysis due to its unique structural features that enable it to act as an effective ligand. Its ability to form stable complexes with various transition metals facilitates the design of highly active and selective catalysts for a wide range of organic transformations. This article delves into specific applications of BDMAEE as a ligand in transition metal catalysis, evaluates its effectiveness through experimental data, and discusses potential future developments.

Chemical Structure and Properties of BDMAEE

Molecular Structure

BDMAEE’s molecular formula is C8H20N2O, with a molecular weight of 146.23 g/mol. The molecule features two tertiary amine functionalities (-N(CH?)?) linked via an ether oxygen atom, which can coordinate with metal centers to stabilize reactive intermediates or enhance catalytic activity.

Physical Properties

BDMAEE is a colorless liquid at room temperature, exhibiting moderate solubility in water but good solubility in many organic solvents. It has a boiling point around 185°C and a melting point of -45°C.

Table 1: Physical Properties of BDMAEE

Mechanism of BDMAEE as a Ligand

Coordination Modes

BDMAEE can coordinate with transition metals through multiple modes, including monodentate, bidentate, or bridging coordination, depending on the nature of the metal and the reaction conditions. These coordination modes influence the electronic and steric properties of the resulting metal complexes, thereby affecting their catalytic performance.

Table 2: Coordination Modes of BDMAEE with Transition Metals

Case Study: Palladium-Catalyzed Suzuki Coupling Reaction

Application: Organic synthesis
Focus: Enhancing catalytic efficiency
Outcome: Achieved high turnover frequency (TOF) and selectivity.

Applications in Transition Metal Catalysis

Cross-Coupling Reactions

One of the most prominent applications of BDMAEE as a ligand is in cross-coupling reactions, where it significantly enhances the efficiency and selectivity of palladium-based catalysts.

Table 3: Performance of BDMAEE in Cross-Coupling Reactions

Case Study: Enhancing the Suzuki-Miyaura Coupling Reaction

Application: Pharmaceutical synthesis
Focus: Improving yield and purity
Outcome: Achieved 95% yield with minimal side products.

Hydrogenation Reactions

BDMAEE also plays a crucial role in hydrogenation reactions, particularly when used as a ligand for rhodium catalysts. It stabilizes the metal center and improves the rate of hydrogenation.

Table 4: Effectiveness of BDMAEE in Hydrogenation Reactions

Case Study: Asymmetric Hydrogenation of Prochiral Ketones

Application: Natural product synthesis
Focus: Enhancing enantioselectivity
Outcome: Achieved 98% ee in the synthesis of complex natural products.

Cycloaddition Reactions

In cycloaddition reactions, BDMAEE coordinates with copper ions to promote the formation of cyclic compounds with high diastereoselectivity.

Table 5: Role of BDMAEE in Cycloaddition Reactions

Case Study: Diels-Alder Reaction Using BDMAEE-Coordinated Copper Complex

Application: Polymer science
Focus: Controlling stereochemistry
Outcome: Produced desired stereoisomer with high selectivity.

Spectroscopic Analysis

Understanding the spectroscopic properties of BDMAEE-metal complexes helps confirm the successful formation of these species and assess their catalytic activity.

Table 6: Spectroscopic Data of BDMAEE-Metal Complexes

Case Study: Confirmation of Metal-Ligand Interaction via NMR

Application: Analytical chemistry
Focus: Verifying complex formation
Outcome: Distinctive NMR peaks confirmed complex formation.

Environmental and Safety Considerations

Handling BDMAEE and BDMAEE-coordinated metal complexes requires adherence to specific guidelines due to potential irritant properties and reactivity concerns. Efforts are ongoing to develop safer handling practices and greener synthesis methods.

Table 7: Environmental and Safety Guidelines

Case Study: Development of Safer Handling Protocols

Application: Industrial safety
Focus: Minimizing risks during handling
Outcome: Implementation of safer protocols without compromising efficiency.

Comparative Analysis with Other Ligands

Comparing BDMAEE with other commonly used ligands such as phosphines and N-heterocyclic carbenes (NHCs) reveals distinct advantages of BDMAEE in terms of efficiency and versatility.

Table 8: Comparison of BDMAEE with Other Ligands

Case Study: BDMAEE vs. Phosphines in Cross-Coupling Reactions

Application: Organic synthesis
Focus: Comparing efficiency and versatility
Outcome: BDMAEE provided superior performance across multiple reactions.

Future Directions and Research Opportunities

Research into BDMAEE continues to explore new possibilities for its use as a ligand in transition metal catalysis. Scientists are investigating ways to further enhance its performance and identify novel applications.

Table 9: Emerging Trends in BDMAEE Research for Catalysis

Case Study: Exploration of BDMAEE in Green Chemistry

Application: Sustainable chemistry practices
Focus: Developing green catalysts
Outcome: Promising results in reducing chemical waste and improving efficiency.

Conclusion

BDMAEE’s distinctive chemical structure endows it with significant capabilities as a ligand in transition metal catalysis, enhancing catalytic activity and selectivity. Understanding its mechanism, efficiency, and applications is crucial for maximizing its utility while ensuring safe and environmentally responsible use. Continued research will undoubtedly uncover additional opportunities for this versatile compound.

References:

1. Smith, J., & Brown, L. (2020). “Synthetic Strategies for N,N-Bis(2-Dimethylaminoethyl) Ether.” Journal of Organic Chemistry, 85(10), 6789-6802.
2. Johnson, M., Davis, P., & White, C. (2021). “Applications of BDMAEE in Polymer Science.” Polymer Reviews, 61(3), 345-367.
3. Lee, S., Kim, H., & Park, J. (2019). “Catalytic Activities of BDMAEE in Organic Transformations.” Catalysis Today, 332, 123-131.
4. Garcia, A., Martinez, E., & Lopez, F. (2022). “Environmental and Safety Aspects of BDMAEE Usage.” Green Chemistry Letters and Reviews, 15(2), 145-152.
5. Wang, Z., Chen, Y., & Liu, X. (2022). “Exploring New Horizons for BDMAEE in Sustainable Chemistry.” ACS Sustainable Chemistry & Engineering, 10(21), 6978-6985.
6. Patel, R., & Kumar, A. (2023). “BDMAEE as a Ligand for Transition Metal Catalysts.” Organic Process Research & Development, 27(4), 567-578.
7. Thompson, D., & Green, M. (2022). “Advances in BDMAEE-Based Ligands for Catalysis.” Chemical Communications, 58(3), 345-347.
8. Anderson, T., & Williams, B. (2021). “Spectroscopic Analysis of BDMAEE Compounds.” Analytical Chemistry, 93(12), 4567-4578.
9. Zhang, L., & Li, W. (2020). “Safety and Environmental Impact of BDMAEE.” Environmental Science & Technology, 54(8), 4567-4578.
10. Moore, K., & Harris, J. (2022). “Emerging Applications of BDMAEE in Green Chemistry.” Green Chemistry, 24(5), 2345-2356.

Extended reading:

High efficiency amine catalyst/Dabco amine catalyst

Non-emissive polyurethane catalyst/Dabco NE1060 catalyst

NT CAT 33LV

NT CAT ZF-10

Dioctyltin dilaurate (DOTDL) – Amine Catalysts (newtopchem.com)

Polycat 12 – Amine Catalysts (newtopchem.com)

Bismuth 2-Ethylhexanoate

Bismuth Octoate

Dabco 2040 catalyst CAS1739-84-0 Evonik Germany – BDMAEE

Dabco BL-11 catalyst CAS3033-62-3 Evonik Germany – BDMAEE