Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Neil Mallo"'
Publikováno v:
Polymer Chemistry. 10:6515-6522
Polymers with donor–acceptor Stenhouse adduct (DASA) groups were synthesized using RAFT methods to evaluate the effect of polymer length (20 vs. 100 DP units) and backbone rigidity (acrylate and methacrylate blocks). A model DASA was not able to sw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcc87926162b8af6fded6cc10ec801f0
https://doi.org/10.1039/c9py01345h
https://doi.org/10.1039/c9py01345h
Autor:
Jonathon E. Beves, Arnaud Tron, Neil Mallo, Jason B. Harper, Joakim Andréasson, Gediminas Jonusauskas, Lorrie S. D. Jacob, Nathan D. McClenaghan
Publikováno v:
ChemPhotoChem
ChemPhotoChem, Wiley, 2020, ⟨10.1002/cptc.201900295⟩
ChemPhotoChem, Wiley, 2020, ⟨10.1002/cptc.201900295⟩
International audience; The binding of donor-acceptor Stenhouse adducts (DASAs) bearing hydrogenbond recognition groups by Hamilton-type receptors significantly influenced their photoswitching properties by altering thermal barriers to isomerization.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d6988f718713fdf509cb8bdfa38d7b3
https://hal.archives-ouvertes.fr/hal-02464386
https://hal.archives-ouvertes.fr/hal-02464386
Publikováno v:
The Journal of organic chemistry. 85(12)
High-level quantum chemical calculations were used to elucidate the gas- and solution-phase conformational equilibria for a series of symmetrically substituted (thio)ureas, (thio)squaramides, and croconamides. Gas-phase calculations predict that the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7a2d37361401cca7e9933027a4a6d5d
https://pubmed.ncbi.nlm.nih.gov/32407087
https://pubmed.ncbi.nlm.nih.gov/32407087
Autor:
Neil Mallo, Jonathon E. Beves, Michael S. Scholz, Eduardo Carrascosa, Gabriel da Silva, James N. Bull, Evan J. Bieske
Publikováno v:
The Journal of Physical Chemistry Letters. 9:665-671
Donor-acceptor Stenhouse adducts (DASAs) are a new class of photoswitching molecules with excellent fatigue resistance and synthetic tunability. Here, tandem ion mobility mass spectrometry coupled with laser excitation is used to characterize the pho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0feaf212a60c63bc3f774b57b31d7df
https://doi.org/10.1021/acs.jpclett.7b03402
https://doi.org/10.1021/acs.jpclett.7b03402
Autor:
Paul L. Burn, Paul E. Shaw, David M. Huang, Wen Liang Tan, Hui Jin, Xuechen Jiao, Aaron M. Raynor, Alex S. Loch, Christopher R. McNeill, Wei Jiang, Neil Mallo, Mohammad Babazadeh
Publikováno v:
Advanced Functional Materials. 32:2104259
Bulk heterojunction organic solar cells continue to show steady photoconversion efficiency improvements. However, single component organic solar cells are a particularly attractive alternative due to the relative simplicity of device manufacture. It
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26d487e92c9e50cf813b256e4a8ed04e
https://doi.org/10.1002/adfm.202104259
https://doi.org/10.1002/adfm.202104259
Autor:
Thomas S. C. MacDonald, Hasti Iranmanesh, Patrick T. Brown, Jonathon E. Beves, Matthew J. Teusner, Neil Mallo, Jason B. Harper, Graham E. Ball
Publikováno v:
Chemical Communications. 52:13576-13579
We report photochromic donor-acceptor Stenhouse adducts (DASAs) capable of fully reversible photoisomerization with visible light in organic solvents including chloroform, acetonitrile and benzene. The rates of photoisomerization and thermal reversio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fe1f6495cf01bd06b95939d5bfbf52e
https://doi.org/10.1039/c6cc08079k
https://doi.org/10.1039/c6cc08079k
Autor:
Jonathon E. Beves, Ena T. Luis, Junming Ho, Eric D.B. Foley, Jason B. Harper, Neil Mallo, Hasti Iranmanesh, Aaron D. W. Kennedy
Publikováno v:
Chemical Science
Surprisingly small structural changes in Donor–Acceptor Stenhouse Adducts (DASAs) result in predictable, robust and effective photochromic switches.
The first in-depth, systematic study of the photoswitching properties of Donor–Acceptor Sten
The first in-depth, systematic study of the photoswitching properties of Donor–Acceptor Sten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f067d380c8f77ee6ebee97a5ceab70e
https://pubmed.ncbi.nlm.nih.gov/30542573
https://pubmed.ncbi.nlm.nih.gov/30542573
Autor:
Jonathan A. Kitchen, Jonathon E. Beves, Samuel V. F. Beddoe, Tony D. Keene, Jason R. Price, Grace G. Morgan, Neil Mallo, Anthony J. Fitzpatrick
Starting with a coordination polymer, {[Cu(L)]2}n (1 where H2L = salicylidene-2-aminophenol), we have explored the ability of polypyridyl ligands (P) to bridge the monomer complex to form nine {[Cu(L)]2(P)} complexes. The identity and solution stabil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3dba679c082b9102bbb176ccee176cd