Results 61 to 70 of about 357,701 (311)

Effect of fungal pre-treatment of poplar chips on its paper brightness reversion [PDF]

open access: yesIranian Journal of Wood and Paper Industries, 2017
Unbleached Kraft pulp made from poplar chips, Pre-treated by Trametes versicolor in 1, 2 and 3 weeks (Bio-Kraft pulp), was used as raw material in this study.
Esmaeil Rasooly Garmaroody   +2 more
doaj  

Carbonyl-Ene Reactions Catalyzed by Bis(oxazoline) Copper (II) Complexes Proceed by a Facile Stepwise Mechanism:  DFT and ONIOM (DFT:PM3) Studies

open access: yes, 2016
The mechanism of a carbonyl-ene addition reaction catalyzed by a bis(oxazoline) copper (II) complex has been studied using DFT methods. We find that the reaction proceeds by a stepwise mechanism with very low barriers and have identified the role of the ...
Iñaki Morao (2509198)   +2 more
core   +1 more source

Intrinsic Photoactive Star ZnPc–Poly(glutamate) Nanoplatforms for Multimodal Glioblastoma Therapy and Brain‐Targeted Delivery

open access: yesAdvanced Functional Materials, EarlyView.
An intrinsic photoactive star‐shaped zinc phtalocyanine‐poly(L‐glutamic acid) (ZnPc‐PGA) nanoplatform for multimodal glioblastoma (GBM) therapy and brain‐targeted elivery. A ZnPc‐PGA‐based multifunctional theranostic nanocarrier platform enables image‐guided, multimodal GBM therapy. ZnPc‐PGA nanocarriers support the integration of fluorescence imaging,
Amina Benaicha‐Fernández   +14 more
wiley   +1 more source

Alcohol and Carbonyl Redox Reactions in Electrochemical Organic Synthesis

open access: yesChemistryEurope
The primary aim of this review is to provide an overview of relevant and efficient methods in organic electrosynthesis, presented in a reader‐friendly format.
Fiammetta Vitulano   +5 more
doaj   +1 more source

13C NMR reveals no evidence of n-π* interactions in proteins. [PDF]

open access: yesPLoS ONE, 2012
An n = π* interaction between neighboring carbonyl groups has been postulated to stabilize protein structures. Such an interaction would affect the (13)C chemical shielding of the carbonyl groups, whose paramagnetic component is dominated by n = π* and π
Bradley Worley   +3 more
doaj   +1 more source

Dipole‐Engineered Conductive Additives for Ultrastable Interphase Evolution in High‐Areal‐Capacity Silicon Anodes

open access: yesAdvanced Functional Materials, EarlyView.
In the work reported herein, dipole‐engineered sulfonated carbon nanofibers enable conductive additives to actively regulate interphase formation in silicon anodes. Polar sulfonyl groups guide electrolyte decomposition to form a compact LiF‐rich interphase while promoting robust integration with silicon.
Song Kyu Kang   +6 more
wiley   +1 more source

C2 to C6 biobased carbonyl platforms for fine chemistry

open access: yesBeilstein Journal of Organic Chemistry
The carbonyl group is central in organic synthesis, thanks to its ability to undergo a vast range of different chemical transformations on its carbon center or at the neighboring positions.
Jingjing Jiang   +4 more
doaj   +1 more source

1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides with Carbonyl Dipolarophiles Yielding Oxazolidine Derivatives

open access: yesMolecules, 2016
We provide a comprehensive account of the 1,3-dipolar cycloaddition reactions of azomethine ylides with carbonyl dipolarophiles. Many different azomethine ylides have been studied, including stabilized and non-stabilized ylides.
Adam G. Meyer, John H. Ryan
doaj   +1 more source

Unified Synthesis of Polycyclic Alkaloids via Complementary Carbonyl Activation

open access: yes, 2021
A complementary dual carbonyl activation strategy for thesynthesis of polycyclic alkaloids has been developed. Successful applications include the synthesis of tetracyclic alkaloids harmalanine, harmalacinine, pentacyclic indoloquinolizidine alkaloid ...
Guoli, He   +2 more
core   +1 more source

Clusterization‐Triggered Emission from Cellulose‐Based Luminophores in Dilute Aqueous Solution through Imine Formation

open access: yesAdvanced Functional Materials, EarlyView.
Clusterization‐triggered emission is realized in dilute aqueous solution by introducing imine linkages into cellulose‐based luminophores. Imine functionalization creates O/N‐rich, hydrogen‐bonded clustered microenvironments that stabilize emissive states and restrict molecular motions. Luminescence is tunable by amine type and multiplicity.
Yazhou Su   +5 more
wiley   +1 more source

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