H2020Individual fellowship2022–2024

GASGOLD · Gold(I)-Catalyzed Polymerization of Acetylene Gas

Horizon 2020 — Marie Skłodowska-Curie Actions

Duration
2022-09-01 → 2024-08-31
EU contribution
€160,932
Participants
1
Scheme
MSCA-IF

Lines connect the coordinator with its partners.

Results in brief

Gold(I)-Catalyzed Polymerization of Acetylene Gas

Acetylene is an inexpensive gaseous reagent that is a major feedstock for chemical synthesis. The small size of acetylene provides a high atom economical potential, well suited for the growing demands of environmentally friendly and financially viable synthetic protocols. The synthesis of 1,3-dienes and oligomeric/polymeric derivatives, such as polyacetylene are examples of current important industrial applications of acetylene. The catalysts used for these processes often struggle with inefficiency and other issues. Acetylene is also highly underutilized in more elaborate organic transformations, such as those catalyzed by transition metals. The incorporation of acetylene as a feedstock in a wider synthetic context will, due to its unique abilities and potential, help tackle current societal environmental and economic challenges. GASGOLD proposes the development of efficient Au(I)-catalyzed methodologies for challenging intermolecular reactions with acetylene to form a range of novel vinylated molecules and important monomers, oligomers and polymers under simple and mild experimental conditions. The success of this project offers innovative solutions and alternative methods to generate previously unobtainable C–C and C–O bonds, in addition to a general improvement of the important transition metal mediated reactions with acetylene, such as the synthesis of 1,3-dienes. Acetylene is a highly important feedstock for chemical industry, with it being used as a starting material for the synthesis of materials such as synthetic rubbers, elastomers and polymer resins. The underutilization of acetylene in more elaborate organic transformations stems from a lack of existing protocols successfully employing acetylene, rather than a supply shortage, with the global demand of acetylene in 2020 being 1.9 million metric tons and it experiences continuous growth. The successful application of acetylene in attractive and innovative synthetic methodologies will provide significant upsides to current synthetic tools due to the low cost, high atom economy and unique reactivity of acetylene. The synthesis of substituted 1,3-dienes have been established using a range of transition metal catalysts, by many of these protocols require harsh reaction conditions, high catalyst loadings, long reaction times and expensive starting materials. Therefore, there is a high demand for methods of the selective synthesis of 1,3-butadiene and other substituted dienes from inexpensive starting materials, such as acetylene gas. GASGOLD aims to generalize and expand on the application of acetylene in transition metal catalyzed methodologies for the challenging application in Au(I)-catalyzed intermolecular cascade synthesis of a range of organic scaffolds stemming from substrates such as alkenes and alcohols. It also aims to improve on the synthesis of 1,3-dienes and related oligomers through divergent reactivity of reaction intermediates formed through the aforementioned Au(I)-catalyzed reaction of acetylene and alkenes.

Data: CORDIS, © European Union

Project objective

GASGOLD aims for the development of efficient Au(I)-catalysed methodologies for the challenging intermolecular synthesis of important monomers, oligomers and polymers of acetylene gas. Au(I)-catalysts allow for the formation of cyclopropyl Au(I)-carbenes after reaction with an alkyne and alkene. The carbenes are reactive towards rearrangement to form 1,3-dienes, which are important building blocks for a range of natural and other important products, such as synthetic rubbers. Preliminary results show that further reaction of certain 1,3-dienes with acetylene can occur, forming oligomeric derivatives and this reactivity will be harnessed and further exploited in this project. Initially, the development of an effective protocol for the synthesis of a wider range and more challenging substituted 1,3-dienes from acetylene gas, both in monomeric and oligomeric forms, will be established. The reaction mechanism determining the configuration of the alkenes will be studied, for example by kinetic monitoring and isolation of reaction intermediates, to explain the observed selectivity, potentially synthesise other isomers and improve on the reaction conditions and catalyst design. The initial results will inspire the challenging selective expansion of 1,3-dienes with acetylene to form substituted 1,3,5-hexatrienes. Additionally, the unprecedented use of both acetylene and ethylene gas in Au(I)-catalysis will be explored for the synthesis of polyacetylene derivatives, which are highly important materials with electrical conductivity, as well as in the purification of ethylene gas. The development of this project offers an innovative solution for the long-standing problem of utilising acetylene gas as a simple building block in Au(I)-catalysis, offering a clear advantage over the current state-of-the-art of the field. Furthermore, the expected synergistic performance between the experienced researcher and the host group, will maximise the potential for success of the project.

Original text from CORDIS.

Participants

  • FUNDACIO INSTITUT CATALA D'INVESTIGACIO QUIMICA · TARRAGONACoordinatorSpain

Links

Data: CORDIS, © European Union