词条 | Harry Anderson (chemist) |
释义 |
|name = Harry Anderson | birth_name = Harry Laurence Anderson |birth_date = {{Birth date and age|df=yes|1964|01|12}} |nationality = United Kingdom |field = Organic chemistry |work_institutions = {{Plainlist|
| thesis_title = Model enzymes based on porphyrins | thesis_year = 1991 | thesis_url = http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.358368 |alma_mater = {{Plainlist|
| honorific_suffix = {{post-nominals |country =GBR |FRS}} | doctoral_advisor = Jeremy Sanders{{citation needed|date=April 2014}} |known_for = Porphyrin Nanorings | website = {{URL|hla.chem.ox.ac.uk}} }}Harry Laurence Anderson, FRS is a British chemist in the Department of Chemistry, University of Oxford. He is well known for his contributions in the syntheses of supramolecular systems (porphyrin nanorings and nanowires) and exploration of the extraordinary physical properties of large pi-conjugated systems. He is a Professor of Chemistry at Keble College, Oxford.[1][2][3] EducationHarry Anderson studied chemistry at Christ Church, University of Oxford, where he received his Bachelor of Arts degree in 1987. This was followed by graduate studies under Jeremy Sanders at the University of Cambridge, where he received his doctoral degree in 1990.[4] Career and ResearchAnderson started his independent research as a research fellow at Magdalene College, Cambridge in 1990–1993, and conducted his research in 1993–1994 as SERC postdoctoral research fellow at ETH-Zürich, Switzerland. He returned to University of Oxford in 1994 as university lecturer in organic chemistry and tutor in Keble College. In 2004, he became professor of chemistry at the University of Oxford. Template directed syntheses ubiquitously exist in nature (protein biosynthesis, etc.), which provides inspiration for synthesising artificial supramolecular systems. Using porphyrin monomers/oligomers and molecular templates of various sizes, porphyrin nanoring systems can be constructed with high versatility.[7][8] These supramolecular systems also bear appealing co-ordination properties, providing inspirations for the co-ordination phenomena existing in nature.[9][10] Vernier templating refers to the syntheses of complexes using templates and molecular building blocks with mismatching co-ordination numbers to construct larger molecular systems by incorporating more than one template molecule and more molecular building blocks than usual. Porphyrin nanoring systems are excellent examples in realising this methodology and giant artificial molecular systems with their molecular weights of small proteins can be constructed.[11][12] Based on the work of organic synthesis, his research interests have found wide range of collaborators from versatile academic backgrounds all over the world. It was found that elongated/encapsulated pi-conjugate systems constructed by porphyrins showed unprecedented physical properties in charge transfer,[13][14] two-photon absorption,[15] etc., thereby providing physicists and photobiologists new candidates and inspirations in their research. Honours and awards
Anderson's nomination for the Royal Society in 2013 reads: {{centred pull quote|Harry Anderson is known internationally for his insightful contributions to the design and synthesis of supramolecular materials and molecular wires. He has introduced new concepts for molecular design, and ground-breaking approaches to template-directed synthesis, leading to materials with unprecedented electronic and nonlinear optical characteristics. He has pioneered the investigation of conjugated porphyrin oligomers, encapsulated pi-systems, nanorings and two-photon absorbing dyes, and he has worked closely with physicists and photobiologists to understand the relationship between molecular structure and function. His work has resulted in profound insights into the factors controlling long-range electronic coupling and charge-transport in supramolecular systems.[17]}} References1. ^{{Scopus id }} {{FRS 2013}}{{Authority control}}{{DEFAULTSORT:Anderson, Harry}}2. ^{{EuropePMC |ORCID =0000-0002-1801-8132}} 3. ^{{cite web |url=http://www.keble.ox.ac.uk/academics/about/professor-h-l-anderson |title=Professor Harry L. Anderson FRS — Keble College |author= |access-date=4 September 2018 }} 4. ^{{cite web|url=http://hla.chem.ox.ac.uk/group/harry.shtml |title=Anderson Research Group@Oxford University |author= |access-date=4 September 2018 }} 5. ^{{Cite journal | doi = 10.1002/anie.199510961| title = Assembly and Crystal Structure of a Photoactive Array of Five Porphyrins| journal = Angewandte Chemie International Edition in English| volume = 34| issue = 10| pages = 1096–1099| year = 1995| last1 = Anderson | first1 = S. | last2 = Anderson | first2 = H. L. | last3 = Bashall | first3 = A. | last4 = McPartlin | first4 = M. | last5 = Sanders | first5 = J. K. M. }} 6. ^{{Cite journal | doi = 10.1039/b010015n| title = Synthesis of fluorescent stilbene and tolan rotaxanes by Suzuki coupling| journal = Chemical Communications| issue = 5| pages = 493–494| year = 2001| last1 = Stanier | first1 = C. A. | last2 = o'Connell | first2 = M. J. | last3 = Anderson | first3 = H. L. | last4 = Clegg | first4 = W. }} 7. ^{{Cite journal | doi = 10.1002/anie.200801188| title = Enhanced π Conjugation around a Porphyrin[6] Nanoring| journal = Angewandte Chemie International Edition| volume = 47| issue = 27| pages = 4993–4996| year = 2008| last1 = Hoffmann | first1 = M. | last2 = Kärnbratt | first2 = J. | last3 = Chang | first3 = M. H. | last4 = Herz | first4 = L. M. | last5 = Albinsson | first5 = B. | last6 = Anderson | first6 = H. L. }} 8. ^{{Cite journal | doi = 10.1002/anie.200604601| title = Template-Directed Synthesis of a π-Conjugated Porphyrin Nanoring| journal = Angewandte Chemie International Edition| volume = 46| issue = 17| pages = 3122–3125| year = 2007| last1 = Hoffmann | first1 = M. | last2 = Wilson | first2 = C. J. | last3 = Odell | first3 = B. | last4 = Anderson | first4 = H. L. }} 9. ^{{Cite journal | doi = 10.1021/ja209254r| title = Stepwise Effective Molarities in Porphyrin Oligomer Complexes: Preorganization Results in Exceptionally Strong Chelate Cooperativity| journal = Journal of the American Chemical Society| volume = 133| issue = 51| pages = 20962–20969| year = 2011| last1 = Hogben | first1 = H. J. | last2 = Sprafke | first2 = J. K. | last3 = Hoffmann | first3 = M. | last4 = Pawlicki | first4 = M. O. | last5 = Anderson | first5 = H. L. | pmid=22091586}} 10. ^{{Cite journal | doi = 10.1002/anie.201008087| title = All-or-Nothing Cooperative Self-Assembly of an Annulene Sandwich| journal = Angewandte Chemie International Edition| volume = 50| issue = 24| pages = 5572–5575| year = 2011| last1 = Sprafke | first1 = J. K. | last2 = Odell | first2 = B. | last3 = Claridge | first3 = T. D. W. | last4 = Anderson | first4 = H. L. | pmid=21544909}} 11. ^{{Cite journal | doi = 10.1038/nature09683| title = Vernier templating and synthesis of a 12-porphyrin nano-ring| journal = Nature| volume = 469| issue = 7328| pages = 72–75| year = 2011| last1 = o'Sullivan | first1 = M. C. | last2 = Sprafke | first2 = J. K. | last3 = Kondratuk | first3 = D. V. | last4 = Rinfray | first4 = C. | last5 = Claridge | first5 = T. D. W. | last6 = Saywell | first6 = A. | last7 = Blunt | first7 = M. O. | last8 = o'Shea | first8 = J. N. | last9 = Beton | first9 = P. H. | last10 = Malfois | first10 = M. | last11 = Anderson | first11 = H. L. | pmid=21209660| bibcode = 2011Natur.469...72O}} 12. ^{{Cite journal | doi = 10.1002/anie.201202870| title = Two Vernier-Templated Routes to a 24-Porphyrin Nanoring| journal = Angewandte Chemie International Edition| volume = 51| issue = 27| pages = 6696–6699| year = 2012| last1 = Kondratuk | first1 = D. V. | last2 = Perdigao | first2 = L. M. A. | last3 = O'Sullivan | first3 = M. C. | last4 = Svatek | first4 = S. | last5 = Smith | first5 = G. | last6 = O'Shea | first6 = J. N. | last7 = Beton | first7 = P. H. | last8 = Anderson | first8 = H. L. | pmid=22653879}} 13. ^{{Cite journal | doi = 10.1038/nnano.2011.111| title = Long-range electron tunnelling in oligo-porphyrin molecular wires| journal = Nature Nanotechnology| volume = 6| issue = 8| pages = 517–23| year = 2011| last1 = Sedghi | first1 = G. | last2 = García-Suárez | first2 = V. C. M. | last3 = Esdaile | first3 = L. J. | last4 = Anderson | first4 = H. L. | last5 = Lambert | first5 = C. J. | last6 = Martín | first6 = S. | last7 = Bethell | first7 = D. | last8 = Higgins | first8 = S. J. | last9 = Elliott | first9 = M. | last10 = Bennett | first10 = N. | last11 = MacDonald | first11 = J. E. | last12 = Nichols | first12 = R. J. | pmid=21804555| bibcode = 2011NatNa...6..517S }} 14. ^{{Cite journal | doi = 10.1039/C3SC22306J| title = "Push-no-pull" porphyrins for second harmonic generation imaging| journal = Chemical Science| volume = 4| issue = 5| pages = 2024| year = 2013| last1 = López-Duarte | first1 = I. | last2 = Reeve | first2 = J. E. | last3 = Pérez-Moreno | first3 = J. | last4 = Boczarow | first4 = I. | last5 = Depotter | first5 = G. | last6 = Fleischhauer | first6 = J. | last7 = Clays | first7 = K. | last8 = Anderson | first8 = H. L. }} 15. ^{{Cite journal | doi = 10.1021/ja901244e| title = Synthesis and Two-Photon Spectrum of a Bis(Porphyrin)-Substituted Squaraine| journal = Journal of the American Chemical Society| volume = 131| issue = 22| pages = 7510–7511| year = 2009| last1 = Odom | first1 = S. A. | last2 = Webster | first2 = S. | last3 = Padilha | first3 = L. A. | last4 = Peceli | first4 = D. | last5 = Hu | first5 = H. | last6 = Nootz | first6 = G. | last7 = Chung | first7 = S. J. | last8 = Ohira | first8 = S. | last9 = Matichak | first9 = J. D. | last10 = Przhonska | first10 = O. V. | last11 = Kachkovski | first11 = A. D. | last12 = Barlow | first12 = S. | last13 = BréDas | first13 = J. L. | last14 = Anderson | first14 = H. L. | last15 = Hagan | first15 = D. J. | last16 = Van Stryland | first16 = E. W. | last17 = Marder | first17 = S. R. | pmid=19435343}} 16. ^https://www.chem.byu.edu/faculty-and-staff/resources/international-symposium-on-macrocyclic-and-supramolecular-chemistry/awards/izatt-christensen-award-recipients/ 17. ^1 {{ cite web |url =http://royalsociety.org/people/harry-anderson/ |title =Professor Harry Anderson FRS |deadurl =yes |archiveurl =https://archive.is/20130705003543/http://royalsociety.org/people/harry-anderson/ |archivedate =5 July 2013 |df =dmy-all }} 18. ^1 {{cite web |url=http://www.rsc.org/ScienceAndTechnology/Awards/SupramolecularChemistryAward/CurrentWinner.asp |title=RSC award archive |deadurl=yes |archiveurl=https://web.archive.org/web/20160304053726/http://www.rsc.org/ScienceAndTechnology/Awards/SupramolecularChemistryAward/CurrentWinner.asp |archivedate=4 March 2016 |df=dmy-all }} 19. ^{{ cite web|url=http://www.rsc.org/Membership/Networking/InterestGroups/Macrocyclic/BobHayLectureship/|title=Bob Hay Lectureship, RSC|deadurl=yes|archiveurl=https://web.archive.org/web/20160304065139/http://www.rsc.org/Membership/Networking/InterestGroups/Macrocyclic/BobHayLectureship/|archivedate=4 March 2016|df=dmy-all}} 20. ^{{cite web |url=http://www.rsc.org/ScienceAndTechnology/Awards/CordayMorganPrizes/PreviousWinners.asp |title=RSC award archive |deadurl=yes |archiveurl=https://web.archive.org/web/20121022001256/http://www.rsc.org/ScienceAndTechnology/Awards/CordayMorganPrizes/PreviousWinners.asp |archivedate=22 October 2012 |df=dmy-all }} 6 : British chemists|Fellows of the Royal Society|Alumni of Christ Church, Oxford|Fellows of Keble College, Oxford|Living people|1964 births |
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