Results 1 to 10 of about 118 (70)

Xylindein: Naturally Produced Fungal Compound for Sustainable (Opto)electronics [PDF]

open access: goldACS Omega, 2019
Organic semiconductors are of interest for (opto)electronic applications due to their low cost, solution processability, and tunable properties. Recently, natural product-derived organic pigments attracted attention due to their extraordinary environmental stability and unexpectedly good optoelectronic performance, in spite of only partially conjugated
Sarath Vega Gutierrez   +2 more
exaly   +6 more sources

Stimulating growth and xylindein production of Chlorociboria aeruginascens in agar-based systems [PDF]

open access: goldAMB Express, 2012
Four isolates of Chlorociboria aeruginascens were tested for possible stimulatory effects when grown on malt agar media containing wood additives. The addition of any of the four types of test wood (Acer saccharum, Populus tremuloides, spalted P.
Daniela Tudor   +2 more
exaly   +7 more sources

Production of natural colorants by liquid fermentation with Chlorociboria aeruginascens and Laetiporus sulphureus and prospective applications [PDF]

open access: yesEngineering in Life Sciences, 2021
The replacement of potentially hazardous synthetic dyes with natural dyes and pigments are of great interest for a sustainable economy. In order to obtain cost‐efficient, environmentally friendly and competitive products, improvements in the cultivation ...
Marlen Zschätzsch   +9 more
doaj   +3 more sources

Optimizing Xylindein from Chlorociboria spp. for (Opto)electronic Applications [PDF]

open access: goldProcesses, 2020
Abstract Xylindein has been isolated from infected wood and several new derivatives have been prepared. Spectroscopic examination of xylindein and its derivatives has established the orientation of the substituents on the central peri-xanthenoxanthene nucleus which has been identified by a mass spectral analysis of the zinc dust distillation product.
Oksana Ostroverkhova   +2 more
exaly   +5 more sources

Preliminary Examination of the Toxicity of Spalting Fungal Pigments: A Comparison between Extraction Methods [PDF]

open access: yesJournal of Fungi (Basel, Switzerland), 2021
Spalting fungal pigments have shown potential in technologies ranging from green energy generation to natural colorants. However, their unknown toxicity has been a barrier to industrial adoption.
Stacey Harper   +2 more
exaly   +4 more sources

Ultrafast Dynamics and Photoresponse of a Fungi‐Derived Pigment Xylindein from Solution to Thin Films

open access: closedChemistry - A European Journal, 2021
AbstractOrganic semiconductor materials have recently gained momentum due to their non‐toxicity, low cost, and sustainability. Xylindein is a remarkably photostable pigment secreted by fungi that grow on decaying wood, and its relatively strong electronic performance is enabled by π–π stacking and hydrogen‐bonding network that promote charge transport.
Taylor Krueger   +2 more
exaly   +5 more sources

Honey as a Xylindein-Stimulatory Media for Chlorociboria Species

open access: goldColorants
Fungi in the Chlorociboria genus produce a blue pigment called xylindein—a pigment with high UV stability, photovoltaic capacity, and which is used as a historic wood colorant.
Olivia Queisser   +4 more
doaj   +3 more sources

Role of Hydroxyl Groups in the Photophysics, Photostability, and (Opto)electronic Properties of the Fungi-Derived Pigment Xylindein

open access: closedJournal of Physical Chemistry C, 2021
Organic semiconductors have attracted increasing attention due to their low cost, solution processability, and tunable properties.
Taylor Krueger   +2 more
exaly   +4 more sources

Xylindein

open access: diamondCHIMIA, 1965
G.M. Blackburn   +2 more
doaj   +4 more sources

The synthesis of 7,9-dimethoxy-3-propyl-3,4-dihydro-1H-benzo[g]isochromene-1,5,10-trione: A potential monomer for the synthesis of the natural product xylindein

open access: diamondArkivoc, 2020
A novel synthesis of a 3-propyl-substituted-benzo[g]isochromene quinone, a potential monomer of the natural product xylindein, was accomplished in 9 steps (overall yield of 8.2%) from 2,4- dimethoxybenzaldehyde. Key steps included the use of a cross-metathesis reaction in which ethyl-3-allyl-4- (benzyloxy)-1,6,8-trimethoxy-2-naphthoate was converted ...
Md. Firoj Hossain   +2 more
openalex   +4 more sources

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