Front cover
Literature Information
The first page of this article is displayed as the abstract.
Related Literature
UO2F2 particulate formation in an impinging jet gas reactor
Joshua A. Hubbard, Meng-Dawn Cheng, Lawrence Cheung, Jared R. Kirsch, Jason M. Richards, Glenn A. Fugate
DOI: 10.1039/D1RE00105A
Hydrogenation of phenol to cyclohexanol using carbon encapsulated Ni–Co alloy nanoparticles
Shuai Wang, Tianhan Zhu, Nan Jiang, Chunlei Zhang, Huan Wang, Yanguang Chen, Feng Li, Hua Song
DOI: 10.1039/D1RE00457C
Correction: Surface reaction kinetics of the methanol synthesis and the water gas shift reaction on Cu/ZnO/Al2O3
Bruno Lacerda de Oliveira Campos, Karla Herrera Delgado, Stefan Wild, Stephan Pitter, Jörg Sauer
DOI: 10.1039/D1RE90031E
Construction of supramolecular laccase enzymes and understanding of catalytic dye degradation using multispectral and molecular docking approaches
Qingteng Zhou, Kaijie Ni, Francesca M. Kerton
DOI: 10.1039/D1RE00111F
Generating molecules with optimized aqueous solubility using iterative graph translation
Camille Bilodeau, Wengong Jin, Hongyun Xu, Jillian A. Emerson, Sukrit Mukhopadhyay, Thomas H. Kalantar, Tommi Jaakkola, Regina Barzilay, Klavs F. Jensen
DOI: 10.1039/D1RE00315A
Methyl acrylatepolymerizations in the presence of a copper/N3S3 macrobicyclic cage in DMSO at 25 °C
Craig A. Bell, Qiao Sun, Hong Zhang, Sean C. Smith, Paul V. Bernhardt, Michael J. Monteiro
DOI: 10.1039/B9PY00315K
A superamplification effect in the detection of explosives by a fluorescent hyperbranched poly(silylenephenylene) with aggregation-enhanced emission characteristics
Yongchun Zhong, Kam Sing Wong
DOI: 10.1039/C0PY00046A
Grafting of polymer brushes from nanopore surface via atom transfer radical polymerization with activators regenerated by electron transfer
Liang Cao, Michal Kruk
DOI: 10.1039/B9PY00282K
Poly(3-hexylthiophene) bearing pendant fullerenes: aggregation vs. self-organization
Bobak Gholamkhass, Timothy J. Peckham, Steven Holdcroft
DOI: 10.1039/B9PY00384C
Activation of β-diketones for CO2 capture and utilization
Khaleel I. Assaf, Abdussalam K. Qaroush, Ibrahim K. Okashah, Feda'a M. Al-Qaisi, Fatima Alsoubani, Ala'a F. Eftaiha
DOI: 10.1039/D1RE00278C
You might also like
What is the market or research trend for N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0)?
N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0) is increasingly being used ...
What precautions should be taken when handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate (CAS: 1050507-06-6)?
When handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate, appropriate p...
What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?
Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...
What is the market or research trend for oxocopper (CAS: 12053-18-8)?
The market for oxocopper (CAS: 12053-18-8) is primarily driven by its use in cat...
What is the market or research trend for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-carboxylic acid?
The market for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-c...
What is 2-(1-Pyrrolidinyl)-4-pyridinamine (CAS: 35981-63-6)?
2-(1-Pyrrolidinyl)-4-pyridinamine is a chemical compound with the CAS number 359...
What are the physical and chemical properties of 2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1)?
2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1) is a crystalline sol...
How is (S)-Alpha-allyl-proline hydrochloride (CAS: 129704-91-2) typically synthesized?
(S)-Alpha-allyl-proline hydrochloride is usually synthesized via a Wittig reacti...
What is 3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5)?
3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5) is an organic compound w...
How is Lys-SMCC-DM1 (CAS: 1281816-04-3) typically synthesized?
Lys-SMCC-DM1 is synthesized via a multi-step process involving the coupling of S...
Source Journal
Analyst

Analyst publishes analytical and bioanalytical research that reports premier fundamental discoveries and inventions, and the applications of those discoveries, unconfined by traditional discipline barriers.














