scholarly article | Q13442814 |
P356 | DOI | 10.1002/CSSC.201500993 |
P698 | PubMed publication ID | 26347029 |
P2093 | author name string | Po-Han Lin | |
Ching-Yuan Liu | |||
Kun-Mu Lee | |||
Deng-Jhou Cai | |||
Te-Jui Lu | |||
P2860 | cites work | A low-cost, high-efficiency solar cell based on dye-sensitized colloidal TiO2 films | Q26778451 |
Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions | Q29012891 | ||
Innate and Guided C–H Functionalization Logic | Q30054500 | ||
Weak coordination as a powerful means for developing broadly useful C-H functionalization reactions | Q30410596 | ||
Catalytic intermolecular direct arylation of perfluorobenzenes. | Q33997391 | ||
Porphyrin-sensitized solar cells with cobalt (II/III)-based redox electrolyte exceed 12 percent efficiency | Q34230064 | ||
Palladium-catalyzed benzene arylation: incorporation of catalytic pivalic acid as a proton shuttle and a key element in catalyst design | Q34592473 | ||
Transition-metal-catalyzed direct arylation of (hetero)arenes by C-H bond cleavage. | Q35016847 | ||
Influence of the donor size in D-π-A organic dyes for dye-sensitized solar cells | Q35127181 | ||
Aryl-aryl bond formation by transition-metal-catalyzed direct arylation. | Q36702962 | ||
Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality | Q37294999 | ||
A general method for copper-catalyzed arylation of arene C-H bonds | Q37339126 | ||
Metal-free organic dyes for dye-sensitized solar cells: from structure: property relationships to design rules | Q37417209 | ||
Direct C-H transformation via iron catalysis | Q37807035 | ||
Towards mild metal-catalyzed C-H bond activation | Q37888484 | ||
Organic sensitizers from D-π-A to D-A-π-A: effect of the internal electron-withdrawing units on molecular absorption, energy levels and photovoltaic performances | Q38063450 | ||
A thieno[3,4-c]pyrrole-4,6-dione-based copolymer for efficient solar cells. | Q43115936 | ||
Engineering of efficient panchromatic sensitizers for nanocrystalline TiO(2)-based solar cells | Q43677273 | ||
Developments in direct C-H arylation of (hetero)arenes under microwave irradiation. | Q45902448 | ||
Synthetic control of structural order in N-alkylthieno[3,4-c]pyrrole-4,6-dione-based polymers for efficient solar cells. | Q45989480 | ||
Conveniently synthesized isophorone dyes for high efficiency dye-sensitized solar cells: tuning photovoltaic performance by structural modification of donor group in donor-pi-acceptor system. | Q46084827 | ||
Establishment of broadly applicable reaction conditions for the palladium-catalyzed direct arylation of heteroatom-containing aromatic compounds | Q46126944 | ||
Starburst triarylamine based dyes for efficient dye-sensitized solar cells. | Q46645005 | ||
Direct arylation of meso-formyl porphyrin | Q46876716 | ||
Dye-sensitized solar cells with 13% efficiency achieved through the molecular engineering of porphyrin sensitizers. | Q48330887 | ||
Cobalt-catalyzed C-H arylations, benzylations, and alkylations with organic electrophiles and beyond. | Q51064285 | ||
Indolo[2,3-b]carbazole synthesized from a double-intramolecular Buchwald-Hartwig reaction: its application for a dianchor DSSC organic dye. | Q51075434 | ||
Molecular engineering of push-pull porphyrin dyes for highly efficient dye-sensitized solar cells: the role of benzene spacers. | Q51754454 | ||
Molecular design principle of all-organic dyes for dye-sensitized solar cells. | Q51825064 | ||
Sensitisation of semiconducting electrodes with ruthenium-based dyes | Q56900953 | ||
Dye-Sensitized Solar Cells | Q58414858 | ||
Catching the Rainbow: Light Harvesting in Dye-Sensitized Solar Cells | Q59480547 | ||
Optimizing Dyes for Dye-Sensitized Solar Cells | Q59480570 | ||
Effect of Anchoring Groups on Single Molecule Charge Transport through Porphyrins | Q62500720 | ||
Acid-Base Equilibria of (2,2'-Bipyridyl-4,4'-dicarboxylic acid)ruthenium(II) Complexes and the Effect of Protonation on Charge-Transfer Sensitization of Nanocrystalline Titania | Q74835064 | ||
Copper-catalyzed aerobic oxidative C-H functionalizations: trends and mechanistic insights | Q82240226 | ||
Bond formations between two nucleophiles: transition metal catalyzed oxidative cross-coupling reactions | Q83463015 | ||
Direct arylation of heteroaromatic compounds with congested, functionalised aryl bromides at low palladium/triphosphane catalyst loading | Q83921516 | ||
Palladium-catalyzed β-selective direct arylation of porphyrins | Q84266910 | ||
A novel D-A-π-A organic sensitizer containing a diketopyrrolopyrrole unit with a branched alkyl chain for highly efficient and stable dye-sensitized solar cells | Q84310988 | ||
Dye-sensitized solar cells based on donor-acceptor π-conjugated fluorescent dyes with a pyridine ring as an electron-withdrawing anchoring group | Q84475681 | ||
Triarylamine: a promising core unit for efficient photovoltaic materials | Q84560925 | ||
Highly Efficient Mesoscopic Dye‐Sensitized Solar Cells Based on Donor–Acceptor‐Substituted Porphyrins | Q84670012 | ||
Enhanced performance of quasi-solid-state dye-sensitized solar cells by branching the linear substituent in sensitizers based on thieno[3,4-c]pyrrole-4,6-dione | Q85229517 | ||
P433 | issue | 19 | |
P921 | main subject | solar cell | Q58803 |
P304 | page(s) | 3222-3227 | |
P577 | publication date | 2015-09-08 | |
P1433 | published in | ChemSusChem | Q2962251 |
P1476 | title | Connecting Direct C-H Arylation Reactions with Dye-Sensitized Solar Cells: A Shortcut to D-A-π-A Organic Dyes. | |
P478 | volume | 8 |
Q91975689 | Combined LCA and Green Metrics Approach for the Sustainability Assessment of an Organic Dye Synthesis on Lab Scale |
Q39062971 | Direct Arylation Strategies in the Synthesis of π-Extended Monomers for Organic Polymeric Solar Cells. |
Q42181195 | Molecular engineering and sequential cosensitization for preventing the "trade-off" effect with photovoltaic enhancement. |
Q48042933 | Sn- and Pd-Free Synthesis of D-π-A Organic Sensitizers for Dye-Sensitized Solar Cells by Cu-Catalyzed Direct Arylation. |
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