Results 71 to 80 of about 51,375 (336)

Crystal structures of (±)-(1SR,5SR,6SR,7SR,10SR,11SR,13RS,14SR)-13-hydroxy-7-methoxymethoxy-11,15,18,18-tetramethyl-3-oxo-2,4-dioxatetracyclo[12.3.1.01,5.06,11]octadec-15-en-10-yl benzoate, its 13-epimer and 13-one derivative

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2015
The title compounds, C29H38O8·0.25C5H12, (A), C29H38O8, (B), and C29H36O8, (C), are tetracyclic benzoates possessing a taxane skeleton with a fused dioxolane ring as the core structure.
Takeshi Oishi   +6 more
doaj   +1 more source

Bromination of Substances Containing two Aromatic Nuclei. Part I. Bromination of Cresyl and Nitropbenyl Benzoates. [PDF]

open access: yes, 1935
Bromination of Substances Containing two Aromatic Nuclei. Part I.
G. v. JADHAV, Y. I. RANGWALA.
core   +1 more source

On‐Water Surface Synthesis of 2D Conjugated Metal–Organic Framework Films With Controllable Layer Orientation Enabling High‐Performance Chemiresistive Sensing

open access: yesAdvanced Materials, EarlyView.
Layer orientation dictates charge transport in 2D conjugated metal–organic frameworks, yet controllable methods remain scarce. We report surfactant monolayer‐assisted on‐water synthesis of cm2‐scale Ni‐HHTP films with programmable face‐on and edge‐on orientations.
Jianjun Zhang   +22 more
wiley   +1 more source

Spatial Orientation‐Dependent Double Hydrogen Bond/Photoredox Cooperative Catalysis in Metal–Organic Frameworks

open access: yesAngewandte Chemie, EarlyView.
We report a heterogeneous double hydrogen bond/photoredox synergistic catalysis, wherein the flexibility and spatial orientation of catalytic centers, rather than catalyst activity, play a dominant role in catalytic performance. ABSTRACT Catalyst activity is typically the primary priority in designing a catalytic system. The higher catalyst activity is
Jing Ouyang   +8 more
wiley   +2 more sources

Intake assessment for benzoates in different subgroups of the Flemish population [PDF]

open access: yes, 2008
An exposure assessment was performed to estimate the daily intake of benzoates for the Flemish population. Three age groups were considered: preschool children (n = 697; age 2-6; 3-day estimated dietary record), adolescents (n = 341; age 14-18; 7-day ...
Maaike Bilau   +8 more
core   +1 more source

Autonomous Locomotion of Tensegrity Structure on Low‐Temperature Surfaces

open access: yesAdvanced Robotics Research, EarlyView.
A low‐temperature responsive tensegrity structure (LRTS) is constructed by integrating low‐responsive temperature liquid crystal elastomer (LCE) cables, nonresponsive cables, and stiff rods. The low phase transition temperature of LCE is achieved by introducing a new liquid crystal mesogen.
Changyue Liu   +5 more
wiley   +1 more source

1.Pyrolytic Studies of Arylimines 2.Synthetic Studies of Natural Products With 2-Phenylbenzofuran framework by the Flash Vacuum Pyrolysis 3.Pyrolytic Studies of Furylmethyl benzoates\ue3Benzothienylmethyl benzoates and N-Methylpyrrolylmethyl benzoates [PDF]

open access: yes, 2011
The thesis is divided into three chapters Chapter 1\ue3Flash vacuum pyrolysis of 2-chloro-N-arenylideneaniline gave quinolines by the intromolecular cyclization.
Hsueh, Yu-Tan
core  

Helix Alignment, Chevrons, and Edge Dislocations in Twist‐Bend Ferroelectric Nematics

open access: yesAdvanced Science, EarlyView.
The recently discovered twist‐bend ferroelectric nematic (NTBF) is the new member of the multiferroic family, representing a fluid with an oblique helicoidal (heliconical) periodic structure of spontaneous electric polarization. The work presents a thorough exploration of the material properties of this phase, how the periodic modulation of ...
Bijaya Basnet   +8 more
wiley   +1 more source

Excited‐State Antiaromaticity in Nonbenzenoid Aromatics: Examining the Dynamics of Intramolecular Proton Transfer With a Small Driving Force

open access: yesAngewandte Chemie, EarlyView.
The excited‐state antiaromaticity of hydroxybenzotropyliums (HBTs) can be tuned through substituent effects to bring the aromatic ‘enol’ (E) and keto (K) tautomers close in energy. This leads to abnormally slow excited‐state proton transfer (on the ns timescale), giving rise to dual fluorescence emission and weak photoacidity.
Promeet K. Saha   +6 more
wiley   +2 more sources

The Reactivity of Benzoates in Mixtures of Water and Aprotic Solvents [PDF]

open access: yes, 2012
Nucleofugalities of pentafluorobenzoate (PFB), 2,4,6-trifluorobenzoate (TFB), 2-nitrobenzoate, and 3,5-dinitrobenzoate (DNB) leaving groups have been derived from the solvolysis rate constants of the corresponding X,Y-substituted Z-benzhydryl benzoates
Kronja, Olga   +5 more
core   +2 more sources

Home - About - Disclaimer - Privacy