Neil G. Pschirer - Publications

Affiliations: 
2001 University of South Carolina, Columbia, SC 

22 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2014 Howard IA, Meister M, Baumeier B, Wonneberger H, Pschirer N, Sens R, Bruder I, Li C, Müllen K, Andrienko D, Laquai F. Two channels of charge generation in perylene monoimide solid-state dye-sensitized solar cells Advanced Energy Materials. 4. DOI: 10.1002/Aenm.201300640  0.466
2013 Meister M, Baumeier B, Pschirer N, Sens R, Bruder I, Laquai F, Andrienko D, Howard IA. Observing charge dynamics in surface reactions by time-resolved stark effects Journal of Physical Chemistry C. 117: 9171-9177. DOI: 10.1021/Jp403268C  0.334
2011 Wonneberger H, Pschirer N, Bruder I, Schöneboom J, Ma CQ, Erk P, Li C, Bäuerle P, Müllen K. Double donor-thiophene dendron-perylene monoimide: efficient light-harvesting metal-free chromophore for solid-state dye-sensitized solar cells. Chemistry, An Asian Journal. 6: 1744-7. PMID 21416617 DOI: 10.1002/Asia.201000895  0.45
2010 Li C, Liu M, Pschirer NG, Baumgarten M, Müllen K. Polyphenylene-based materials for organic photovoltaics. Chemical Reviews. 110: 6817-55. PMID 20583837 DOI: 10.1021/Cr100052Z  0.373
2009 Li C, Schöneboom J, Liu Z, Pschirer NG, Erk P, Herrmann A, Müllen K. Rainbow perylene monoimides: easy control of optical properties. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 878-84. PMID 19072796 DOI: 10.1002/Chem.200802126  0.471
2009 Li C, Liu Z, Schöneboom J, Eickemeyer F, Pschirer NG, Erk P, Herrmann A, Müllen K. Perylenes as sensitizers in hybrid solar cells: how molecular size influences performance Journal of Materials Chemistry. 19: 5405. DOI: 10.1039/B823498A  0.378
2009 Edvinsson T, Pschirer N, Schöneboom J, Eickemeyer F, Boschloo G, Hagfeldt A. Photoinduced electron transfer from a terrylene dye to TiO2: Quantification of band edge shift effects Chemical Physics. 357: 124-131. DOI: 10.1016/J.Chemphys.2008.11.024  0.358
2008 Zhou G, Pschirer N, Schöneboom JC, Eickemeyer F, Baumgarten M, Müllen K. Ladder-Type Pentaphenylene Dyes for Dye-Sensitized Solar Cells Chemistry of Materials. 20: 1808-1815. DOI: 10.1021/Cm703459P  0.395
2006 Pschirer NG, Kohl C, Nolde F, Qu J, Müllen K. Pentarylene- and hexarylenebis(dicarboximide)s: near-infrared-absorbing polyaromatic dyes. Angewandte Chemie (International Ed. in English). 45: 1401-4. PMID 16425337 DOI: 10.1002/anie.200502998  0.333
2005 Nolde F, Qu J, Kohl C, Pschirer NG, Reuther E, Müllen K. Synthesis and modification of terrylenediimides as high-performance fluorescent dyes. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 3959-67. PMID 15844133 DOI: 10.1002/chem.200401177  0.416
2004 Qu J, Pschirer NG, Liu D, Stefan A, De Schryver FC, Müllen K. Dendronized perylenetetracarboxdiimides with peripheral triphenylamines for intramolecular energy and electron transfer. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 528-37. PMID 14735521 DOI: 10.1002/chem.200304994  0.378
2003 Chapman CT, Goforth AM, Pschirer NG, Smith MD, Bunz UHF, Zur Loye HC. Synthesis and crystal structure of catena-poly[Rh2(OAc) 4(C27H15N3)]·2CH 2Cl2, a novel Rh(II) organic/inorganic coordination polymer Journal of Chemical Crystallography. 33: 885-890. DOI: 10.1023/A:1027414030899  0.352
2002 Pschirer NG, Ciurtin DM, Smith MD, Bunz UHF, Zur Loye HC. Noninterpenetrating square-grid coordination polymers with dimensions of 25 × 25 Å2 prepared by using N,N′-type ligands: The first chiral square-grid coordination polymer Angewandte Chemie - International Edition. 41: 583-585. DOI: 10.1002/1521-3773(20020215)41:4<583::Aid-Anie583>3.0.Co;2-I  0.348
2001 Pschirer NG, Byrd K, Bunz UHF. Fluorenone-containing poly(p-phenyleneethynylene)s (PPE) and poly(fluorenyleneethynylene)s (PFE): Tuning the solid-state emission of alkyne-bridged polymers by interchain energy transfer Macromolecules. 34: 8590-8592. DOI: 10.1021/Ma011330M  0.355
2001 Ciurtin DM, Pschirer NG, Smith MD, Bunz UHF, Zur Loye HC. Two luminescent coordination polymers with a triple-helix structure: HgX2(C31H24N2) ·CH2Cl2 (X = Cl and Br) Chemistry of Materials. 13: 2743-2745. DOI: 10.1021/Cm0103545  0.366
2001 Brizius G, Pschirer NG, Steffen W, Stitzer K, zur Loye H, Bunz UHF. ChemInform Abstract: Alkyne Metathesis with Simple Catalyst Systems: Efficient Synthesis of Conjugated Polymers Containing Vinyl Groups in Main or Side Chain. Cheminform. 32: no-no. DOI: 10.1002/chin.200115044  0.547
2000 Pschirer NG, Fu W, Adams RD, Bunz UHF. Ring-closing alkyne metathesis with simple catalyst systems: an access to molecular triangles and rhomboids Chemical Communications. 87-88. DOI: 10.1039/A908638B  0.334
2000 Pschirer NG, Vaughn ME, Dong YB, Loye Hz, Bunz UHF. Novel liquid-crystalline PPE-naphthalene copolymers displaying blue solid-state fluorescence Chemical Communications. 85-86. DOI: 10.1039/A907479A  0.364
2000 Brizius G, Pschirer NG, Steffen W, Stitzer K, zur Loye H, Bunz UHF. Alkyne Metathesis with Simple Catalyst Systems:  Efficient Synthesis of Conjugated Polymers Containing Vinyl Groups in Main or Side Chain Journal of the American Chemical Society. 122: 12435-12440. DOI: 10.1021/Ja0010251  0.58
2000 Pschirer NG, Marshall AR, Stanley C, Beckham HW, Bunz UHF. Synthesis and characterization of poly[1,5-(3,7-di-tert-butyl)naphthyleneethynylene] by alkyne metathesis Macromolecular Rapid Communications. 21: 493-495. DOI: 10.1002/(Sici)1521-3927(20000501)21:8<493::Aid-Marc493>3.0.Co;2-S  0.424
1999 Dong Y, Layland RC, Smith MD, Pschirer NG, Bunz UHF, zur Loye H. Syntheses and Characterizations of One-Dimensional Coordination Polymers Generated from Cadmium Nitrate and Bipyridine Ligands Inorganic Chemistry. 38: 3056-3060. DOI: 10.1021/Ic9814569  0.325
1999 Pschirer NG, Bunz UH. Alkyne metathesis with simple catalyst systems: High yield dimerization of propynylated aromatics; scope and limitations Tetrahedron Letters. 40: 2481-2484. DOI: 10.1016/S0040-4039(99)00282-8  0.521
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