H2020Individual fellowship2016–2018

IminoBoron · Iminoboronate polymers as dynamic smart materials

Horizon 2020 — Marie Skłodowska-Curie Actions

Duration
2016-03-01 → 2018-02-28
EU contribution
€195,455
Participants
1
Scheme
MSCA-IF

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Results in brief

Iminoboronate polymers as dynamic smart materials

The aim of this project is the formation of a new class of dynamic, conjugated polymers based on a reversible conjugated polyimine backbone with pendant boronic acids. Monomers incorporating aldehyde, amines and boronic acid functionalities will condense together to construct the polymer backbone. Further functionalization by formation of boronate esters with diols will constitute the key tool to tuning the properties of the polymer. The presence of the two independently interchangeable dynamic covalent bonds (imine and boronate ester) opens the door to new functional material able to respond to two orthogonal external stimuli. In regards of the applications, our objectives are dual: firstly, we will prepare highly tunable materials with promising electronic properties, structural rigidity, which comes from the dative N→B stabilisation, and electrochemical stability, as a consequence of the non-conjugated boron functionalization, which renders them strong candidates for use in light-emitting devices. We aim to succeed in the construction of new conjugated and easily processable blue-light emitting polymers that will take a leading role on the next generation of multifunctional OLED devices, leading to a more sustainable energy consumption. Secondly, conjugated polymers with chemical receptors directly attached to the polymer backbone can act as highly sensitive fluorescent chemosensors. The dynamism of the iminoboronate polymers also renders them as promising candidates for sensing applications. Their projected sensitivity is ascribed to electronic communication between receptors, via the conjugated backbone. Moreover, the reversible formation of cyclic boronates between boronic acid functional polymers and diols has been extensively used in saccharide and anion recognition. We will focus our attention on glucose, which is directly related to diabetes, a disease that is becoming alarmingly common in our society. All the synthetic effort put into this project has led us to understand and establish the methods and procedures by which smart iminoboronate-based polymers can be accessible. Therefore, we have gained the necessary knowledge to successfully synthesise iminoboronate polymers and we are now in the position of effectively designing new structures to overcome the solubility problems that we have faced in the past, and therefore, construct the desired devices.

Data: CORDIS, © European Union

Project objective

Dynamic polymers, which are able to break and reform due to the dynamic nature of their linkages, can be considered as a new class of smart materials, since they can be altered and/or respond to different external stimuli. We propose a new class of dynamic, conjugated polymers based on the reversible iminoboronate ester bonding motif. Simple monomers containing aldehyde, amine, and boronic acid functionalities will polymerize together with diols to produce iminoboronate ester polymers. The presence of orthogonal dynamic imine and boronate ester bonds will allow us to develop easily functionalizable, and thus tuneable, multicomponent polymer materials that possess the ability to reorganise or adapt in response to various external stimuli. The incorporation of electronically distinct diols, will permit us to tune the photophysical and chemical properties of the conjugated polyimine polymer backbone, enabling the possibility to attain the desired material properties. These multifunctional materials will be investigated as fluorescent polyreceptors for specific diols and as controllably crosslinkable or decrosslinkable materials with the addition or displacement of tetrols. Moreover, development of these high-value smart materials will lay the groundwork for the next generation of multifunctional devices, such as blue-light-emitting polymers with superior efficiency and electrochemical stability to the state-of-the-art poly(fluorene) and GaN (O)LEDs.

Original text from CORDIS.

Participants

  • THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE · CAMBRIDGECoordinatorUnited Kingdom

Links

Data: CORDIS, © European Union