TY  - JOUR
AU  - Xiao, Yu
AU  - Yue, Tian-Jun
AU  - Lu, Xiao-Bing
AU  - Ren, Wei-Min
TI  - Stereoregular poly(2-phenylthiirane) via cationic ring-opening polymerization
JF  - CHEMICAL COMMUNICATIONS
J2  - CHEM COMMUN
PY  - 2024
SN  - 1359-7345
DO  - 10.1039/D4CC01281J
UR  - https://m2.mtmt.hu/api/publication/34804214
ID  - 34804214
AB  - Herein, we describe an effective strategy for synthesizing polythioethers with a well-defined structure through the cationic polymerization of thiirane with electron-withdrawing substituents.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Garner, Marc H.
AU  - Blaskovits, J. Terence
AU  - Corminboeuf, Clemence
TI  - Enhanced inverted singlet-triplet gaps in azaphenalenes and non-alternant hydrocarbons
JF  - CHEMICAL COMMUNICATIONS
J2  - CHEM COMMUN
PY  - 2024
PG  - 4
SN  - 1359-7345
DO  - 10.1039/d3cc05747j
UR  - https://m2.mtmt.hu/api/publication/34658399
ID  - 34658399
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Ahlawat, Monika
AU  - Rao, Vishal Govind
TI  - Insights into interfacial mechanisms: CsPbBr<sub>3</sub> nanocrystals as sustainable photocatalysts for primary amine oxidation
JF  - CHEMICAL COMMUNICATIONS
J2  - CHEM COMMUN
PY  - 2024
PG  - 4
SN  - 1359-7345
DO  - 10.1039/d3cc05725a
UR  - https://m2.mtmt.hu/api/publication/34651210
ID  - 34651210
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Maier, Karley B.
AU  - Rust, Lauren N.
AU  - Carniato, Fabio
AU  - Botta, Mauro
AU  - Woods, Mark
TI  - α-Aryl substituted GdDOTA derivatives, the perfect contrast agents for MRI?
JF  - CHEMICAL COMMUNICATIONS
J2  - CHEM COMMUN
PY  - 2024
PG  - 4
SN  - 1359-7345
DO  - 10.1039/d3cc05989h
UR  - https://m2.mtmt.hu/api/publication/34594494
ID  - 34594494
AB  - Enhancing the performance of Gd3+ chelates as relaxation agents for MRI has the potential to lower doses, improving safety and mitigating the environmental impact on our surface waters. More than three decades of research into manipulating the properties of Gd3+ have failed to develop a chelate that simultaneously optimizes all relevant parameters and affords maximal relaxivity. Introducing aryl substituents into the alpha-position of the pendant arms of a GdDOTA chelate affords chelates that, for the first time, simultaneously optimize all physico-chemical properties. Slowing tumbling by binding to human serum albumin affords a relaxivity of 110 +/- 5 mM-1 s-1, close to the maximum possible. As discrete chelates, these alpha-aryl substituted GdDOTA chelates exhibit relaxivities that are 2-3 times higher than those of currently used agents, even at the higher fields (1.5 & 3.0 T) used in modern clinical MRI.Introducing aryl substituents into the alpha-position of the well-known GdDOTA affords chelates that have unprecedentedly high relaxivities and robustness.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Ju, S.
AU  - Zhang, C.
AU  - Tang, B.
AU  - Liu, L.L.
AU  - Stephan, D.W.
AU  - Wu, Y.
TI  - The Lewis Superacidic Aluminium Cation: [(NHC)Al(C6F5)2]+
JF  - CHEMICAL COMMUNICATIONS
J2  - CHEM COMMUN
PY  - 2024
SP  - 698
EP  - 701
PG  - 4
SN  - 1359-7345
UR  - https://m2.mtmt.hu/api/publication/34524715
ID  - 34524715
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Meng, X.
AU  - Dong, Y.
AU  - Liu, Q.
AU  - Wang, W.
TI  - Organophotocatalytic α-deuteration of unprotected primary amines via H/D exchange with D2O
JF  - CHEMICAL COMMUNICATIONS
J2  - CHEM COMMUN
VL  - 60
PY  - 2024
SP  - 296
EP  - 299
PG  - 4
SN  - 1359-7345
DO  - 10.1039/d3cc04634f
UR  - https://m2.mtmt.hu/api/publication/34437815
ID  - 34437815
N1  - Department of Pharmacology and Toxicology, R. Ken Coit College of Pharmacy, University of Arizona, United States            
            Department of Chemistry and Biochemistry, University of Arizona, United States            
            University of Arizona Cancer Centre, University of Arizona, 1703 E. Mabel Street, Tucson, AZ 85721-0207, United States            
            Export Date: 15 December 2023            
            CODEN: CHCOF            
            Correspondence Address: Wang, W.; Department of Pharmacology and Toxicology, United States; email: weiwang1@arizona.edu
AB  - We report a straightforward H/D exchange method for the synthesis of α-deuterated primary amines from a diverse set of primary amines with high levels of deuteration and chemo- and site selectivity and preparative utility. This cost-effective strategy enables the direct conversion of primary amines to α-deuterated counterparts using D2O as the deuterium source under mild reaction conditions without requiring additional functionality manipulation and with minimal byproduct production. © 2024 The Royal Society of Chemistry.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Liu, Rui
AU  - Mondal, Kartik Chandra
AU  - Wang, Chenfeng
AU  - Suthar, Sonam
AU  - Fang, Zijie
AU  - Zuo, Darui
AU  - Li, Yan
TI  - Synthesis of SiN/SiS-heterocycles via the reactions of a bis-silylene with isocyanate/isothiocyanate molecules
JF  - CHEMICAL COMMUNICATIONS
J2  - CHEM COMMUN
VL  - 60
PY  - 2024
IS  - 9
SP  - 1148
EP  - 1151
PG  - 4
SN  - 1359-7345
DO  - 10.1039/d3cc04950g
UR  - https://m2.mtmt.hu/api/publication/34619878
ID  - 34619878
AB  - Reactions of o-carborane-fused bis-silylene 1 with isocyanate/isothiocyanate molecules furnished a series of SiN/SiS-heterocycles, which show distinct styles of cyclization and were theoretically studied.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Bao, Yu
AU  - Zhou, Wenqin
AU  - Miao, Wenhui
AU  - Jia, Guoqing
AU  - Li, Can
TI  - Dopamine oxidation promoted by human telomeric DNA models in the presence of a Cu(<sc>ii</sc>) terpyridine chelate
JF  - CHEMICAL COMMUNICATIONS
J2  - CHEM COMMUN
VL  - 60
PY  - 2024
IS  - 9
SP  - 1172
EP  - 1175
PG  - 4
SN  - 1359-7345
DO  - 10.1039/d3cc05530b
UR  - https://m2.mtmt.hu/api/publication/34600625
ID  - 34600625
AB  - We found that under oxidative stress conditions, the coexistence of human telomeric DNA (HT-DNA) and a copper-terpyridine metallodrug can accelerate dopamine oxidation. The unwinding of HT-DNA from a duplex to cytosine-rich (C-rich) and guanine-rich (G-rich) single strands promotes dopamine oxidation in a general order of C-rich > G-rich > duplex. Along with dopamine oxidation, HT-DNA also undergoes severe damage.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Bugg, Timothy D. H.
TI  - The chemical logic of enzymatic lignin degradation
JF  - CHEMICAL COMMUNICATIONS
J2  - CHEM COMMUN
VL  - 60
PY  - 2024
IS  - 7
SP  - 804
EP  - 814
PG  - 11
SN  - 1359-7345
DO  - 10.1039/d3cc05298b
UR  - https://m2.mtmt.hu/api/publication/34659541
ID  - 34659541
N1  - Export Date: 13 March 2024            
            CODEN: CHCOF            
            Correspondence Address: Bugg, T.D.H.; Department of Chemistry, United Kingdom; email: T.D.Bugg@warwick.ac.uk
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Zhou, Weinan
AU  - Lavendomme, Roy
AU  - Zhang, Dawei
TI  - Recent progress in iodine capture by macrocycles and cages
JF  - CHEMICAL COMMUNICATIONS
J2  - CHEM COMMUN
VL  - 60
PY  - 2024
IS  - 7
SP  - 779
EP  - 792
PG  - 14
SN  - 1359-7345
DO  - 10.1039/d3cc05337g
UR  - https://m2.mtmt.hu/api/publication/34648757
ID  - 34648757
LA  - English
DB  - MTMT
ER  -