Zobrazeno 1 - 10
of 80
pro vyhledávání: '"Benjamin J. Whitaker"'
Autor:
Benjamin J. Whitaker
Charged particle imaging has revolutionized experimental studies of photodissociation and bimolecular collisions. Written in a tutorial style by some of the key practitioners in the field, this book gives a comprehensive account of the technique and
Autor:
Daniel J. Tate, Rémi Anémian, Richard J. Bushby, Suwat Nanan, Stuart L. Warriner, and Benjamin J. Whitaker
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 120-128 (2012)
It has been shown that the base-initiated cyclo-oligomerisation of phthalonitriles is favoured by bulky α-substituents making it possible to obtain the metal-free phthalocyanine directly and in high yield. The phthalocyanine with eight α-isoheptyl
Externí odkaz:
https://doaj.org/article/26df86d3943a4e348ce25510c583aeac
Publikováno v:
The Journal of Physical Chemistry C. 118:24102-24109
We consider the highly radiative, long-lived photoluminescence (PL) component observed in colloidal CuInS2/ZnS core/shell quantum dots (CIS/ZnS QDs) and provide evidence of the involvement of intragap defect states in the emission, settling a long on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65e4371b1fbe55b1a18c306b45beebae
https://doi.org/10.1021/jp5065374
https://doi.org/10.1021/jp5065374
Publikováno v:
Journal of computational chemistry. 37(18)
Since the discovery of the halogen dance (HD) reaction more than 60 years ago, numerous insights into the mechanism have been unveiled. To date however, the reaction has not been investigated from a theoretical perspective. Density functional theory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c50669a1b0afca7d13b8487e77296582
https://pubmed.ncbi.nlm.nih.gov/27075112
https://pubmed.ncbi.nlm.nih.gov/27075112
Autor:
Khalid M. Siddiqui, Stuart A. Hayes, R. J. Dwayne Miller, Benjamin J. Whitaker, Andreas Rossos, R. Scott Murphy, Gastón Corthey, Rui Xian, Daniel Salvatore Badali
Publikováno v:
CrystEngComm 18(38), 7212-7216 (2016). doi:10.1039/C6CE01049K
CrystEngComm
CrystEngComm
CrystEngComm 18(38), 7212 - 7216(2016). doi:10.1039/C6CE01049K
Reversibility is an important issue that prevents ultrafast studies of chemical reactions in solid state due to product accumulation. Here we present an approach that makes use of sp
Reversibility is an important issue that prevents ultrafast studies of chemical reactions in solid state due to product accumulation. Here we present an approach that makes use of sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82cac2c60b32d1f659736d25d14ddb3e
https://bib-pubdb1.desy.de/record/307530
https://bib-pubdb1.desy.de/record/307530
Autor:
Richard J. Bushby, Stuart L. Warriner, Daniel J. Tate, Rémi Anémian, and Benjamin J Whitaker, Suwat Nanan
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 120-128 (2012)
Beilstein Journal of Organic Chemistry
Tate, D J, Anémian, R, Bushby, R J, Nanan, S, Warriner, S L & Whitaker, B J 2012, ' Improved syntheses of high hole mobility phthalocyanines: A case of steric assistance in the cyclo-oligomerisation of phthalonitriles ', Beilstein Journal of Organic Chemistry, vol. 8, pp. 120-128 . https://doi.org/10.3762/bjoc.8.14
Beilstein Journal of Organic Chemistry
Tate, D J, Anémian, R, Bushby, R J, Nanan, S, Warriner, S L & Whitaker, B J 2012, ' Improved syntheses of high hole mobility phthalocyanines: A case of steric assistance in the cyclo-oligomerisation of phthalonitriles ', Beilstein Journal of Organic Chemistry, vol. 8, pp. 120-128 . https://doi.org/10.3762/bjoc.8.14
It has been shown that the base-initiated cyclo-oligomerisation of phthalonitriles is favoured by bulky α-substituents making it possible to obtain the metal-free phthalocyanine directly and in high yield. The phthalocyanine with eight α-isoheptyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bb597c04cf7f4d4af6761c9d5e2575b
https://doaj.org/article/26df86d3943a4e348ce25510c583aeac
https://doaj.org/article/26df86d3943a4e348ce25510c583aeac
Publikováno v:
Journal of Modern Optics. 55:197-209
A representation of the search space in optical pulse shaping problems employing an acousto-optic programmable dispersive filter (AOPDF) is presented for use in closed-loop learning experiments where the optimal spectral phase function to some contro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7232f7c2dc47d7b0dcd573c31ad3c6ce
https://doi.org/10.1080/09500340701363166
https://doi.org/10.1080/09500340701363166
Publikováno v:
Chemical Physics Letters. 427:317-321
Phase modulated light pulses from a non-collinear optical parametric amplifier are used to manipulate the fluorescence intensity of a dye in ethanol solution. The spectrum of the exciting light is centered well to the red of the absorption spectrum o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a400aa208b8153a8e7046cc1adf6d77a
https://doi.org/10.1016/j.cplett.2006.07.006
https://doi.org/10.1016/j.cplett.2006.07.006
Publikováno v:
The Journal of Physical Chemistry A. 108:6823-6835
Femtosecond time-resolved photoelectron imaging (TR-PEI) is applied to the (1 + 2‘) resonance-enhanced multiphoton ionization of pyrazine (1,4-diazabenzene) via the S1 state. The intersystem crossing (ISC) from the S1 (nπ*) to the T1 (nπ*) state
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46e3defd282319126c650bd56a6110cf
https://doi.org/10.1021/jp0484985
https://doi.org/10.1021/jp0484985
Autor:
John Griffiths, Benjamin J. Whitaker
Publikováno v:
Combustion and Flame. 131:386-399
Experiments have been performed in a rapid compression machine to investigate the conditions for and the origins of “knock” in controlled autoignition (CAI), or homogeneous charge compression ignition (HCCI). The combustion of n-pentane in air at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa1e8dc887edd57acea8644470e350fa
https://doi.org/10.1016/s0010-2180(02)00417-0
https://doi.org/10.1016/s0010-2180(02)00417-0