26 research outputs found
Development of a More Sustainable Appel Reaction
Herein,
we report a green, chromatography-free Appel chlorination
and bromination in both catalytic and stoichiometric form. Improved
sustainability was achieved via the effective replacement of chlorinated
solvents with dimethyl carbonate and the use of triphenylphosphine
oxide (PPh3O) as a recyclable organocatalyst. The substrate
scope of this halogenated solvent-free reaction was shown to be analogous
to a contemporary methodology, and removal and recovery of PPh3O from the desired products were effectively demonstrated.
Investigations into the catalytic cycle were conducted, and REACT-IR
was demonstrated to be an effective method of reaction monitoring
in situ. Optimized methodology was applied to the synthesis of 1-bromo-4-(1-bromoethyl)benzene,
a key building block employed during the discovery of a GSK fatty
acid synthase inhibitor
Development of a More Sustainable Appel Reaction
Herein,
we report a green, chromatography-free Appel chlorination
and bromination in both catalytic and stoichiometric form. Improved
sustainability was achieved via the effective replacement of chlorinated
solvents with dimethyl carbonate and the use of triphenylphosphine
oxide (PPh3O) as a recyclable organocatalyst. The substrate
scope of this halogenated solvent-free reaction was shown to be analogous
to a contemporary methodology, and removal and recovery of PPh3O from the desired products were effectively demonstrated.
Investigations into the catalytic cycle were conducted, and REACT-IR
was demonstrated to be an effective method of reaction monitoring
in situ. Optimized methodology was applied to the synthesis of 1-bromo-4-(1-bromoethyl)benzene,
a key building block employed during the discovery of a GSK fatty
acid synthase inhibitor
Supplementary document for Supergrowth and sub-wavelength object imaging - 6587927.pdf
Intensity calculation
Supplementary document for Enhanced on-chip frequency measurement using weak value amplification - 5474937.pdf
Description of numerical methods used in the main pape
Replacement of Less-Preferred Dipolar Aprotic and Ethereal Solvents in Synthetic Organic Chemistry with More Sustainable Alternatives
Dipolar aprotic and ethereal solvents
comprise just over 40% of
all organic solvents utilized in synthetic organic, medicinal, and
process chemistry. Unfortunately, many of the common “go-to”
solvents are considered to be “less-preferable” for
a number of environmental, health, and safety (EHS) reasons such as
toxicity, mutagenicity, carcinogenicity, or for practical handling
reasons such as flammability and volatility. Recent legislative changes
have initiated the implementation of restrictions on the use of many
of the commonly employed dipolar aprotic solvents such as dimethylformamide
(DMF) and N-methyl-2-pyrrolidinone (NMP), and for
ethers such as 1,4-dioxane. Thus, with growing legislative, EHS, and
societal pressures, the need to identify and implement the use of
alternative solvents that are greener, safer, and more sustainable
has never been greater. Within this review, the ubiquitous nature
of dipolar aprotic and ethereal solvents is discussed with respect
to the physicochemical properties that have made them so appealing
to synthetic chemists. An overview of the current legislative restrictions
being imposed on the use of dipolar aprotic and ethereal solvents
is discussed. A variety of alternative, safer, and more sustainable
solvents that have garnered attention over the past decade are then
examined, and case studies and examples where less-preferable solvents
have been successfully replaced with a safer and more sustainable
alternative are highlighted. Finally, a general overview and guidance
for solvent selection and replacement are included in the Supporting
Information of this review
Replacement of Less-Preferred Dipolar Aprotic and Ethereal Solvents in Synthetic Organic Chemistry with More Sustainable Alternatives
Dipolar aprotic and ethereal solvents
comprise just over 40% of
all organic solvents utilized in synthetic organic, medicinal, and
process chemistry. Unfortunately, many of the common “go-to”
solvents are considered to be “less-preferable” for
a number of environmental, health, and safety (EHS) reasons such as
toxicity, mutagenicity, carcinogenicity, or for practical handling
reasons such as flammability and volatility. Recent legislative changes
have initiated the implementation of restrictions on the use of many
of the commonly employed dipolar aprotic solvents such as dimethylformamide
(DMF) and N-methyl-2-pyrrolidinone (NMP), and for
ethers such as 1,4-dioxane. Thus, with growing legislative, EHS, and
societal pressures, the need to identify and implement the use of
alternative solvents that are greener, safer, and more sustainable
has never been greater. Within this review, the ubiquitous nature
of dipolar aprotic and ethereal solvents is discussed with respect
to the physicochemical properties that have made them so appealing
to synthetic chemists. An overview of the current legislative restrictions
being imposed on the use of dipolar aprotic and ethereal solvents
is discussed. A variety of alternative, safer, and more sustainable
solvents that have garnered attention over the past decade are then
examined, and case studies and examples where less-preferable solvents
have been successfully replaced with a safer and more sustainable
alternative are highlighted. Finally, a general overview and guidance
for solvent selection and replacement are included in the Supporting
Information of this review
Experiments in climate governance – lessons from a systematic review of case studies in transition research
Experimentation has been proposed as one of the ways in which public policy can drive sustainability transitions, notably by creating or delimiting space for experimenting with innovative solutions to sustainability challenges. In this paper we report on a systematic review of articles published between 2009 and 2015 that have addressed experiments aiming either at understanding decarbonisation transitions or enhancing climate resilience. Using the case survey method, we find few empirical descriptions of real-world experiments in climate and energy contexts in the scholarly literature, being observed in only 25 articles containing 29 experiments. We discuss the objectives, outputs and outcomes of these experiments noting that explicit experimenting with climate policies could be identified only in 12 cases. Based on the results we suggest a definition of climate policy experiments and a typology of experiments for sustainability transitions that can be used to better understand the role of and learn more effectively from experiments in sustainability transitions
Experiments in climate governance – a systematic review of research on energy and built environment transitions
Experimentation has been proposed as a key way in which governance drives sustainability transitions, notably by creating space for innovative solutions to emerge. In seeking to bring greater coherence to the literatures on climate and sustainability governance experiments, this article reports on a systematic review of articles published between 2009 and 2015. Based on these results a new definition and typology of climate governance experiments is suggested. The typology distinguishes between the various purposes experiments can have, including niche creation, market creation, spatial development, and societal problem solving. It deepens the understanding of the diversity in experimenting by highlighting the salient features of different types of governance experiments. It can therefore guide future research to generate more cumulative research findings contributing to a better understanding of the role and outcomes of experiments in societal transitions. The findings also suggests that real transitions towards low-carbon and climate-resilient societies will require a systematic deliberate combination of different types of experiments
