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Vladimir N Nesterov

Explore the profile of Vladimir N Nesterov including associated specialties, affiliations and a list of published articles. Areas
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Articles 67
Citations 159
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Recent Articles
1.
Lu Z, Luciani L, Li S, Nesterov V, Zuccaccia C, Macchioni A, et al.
Chemistry . 2024 May; 30(51):e202401576. PMID: 38735852
A yet-outstanding supramolecular chemistry challenge is isolation of novel varieties of stacked complexes with finely-tuned donor-acceptor bonding and optoelectronic properties, as herein reported for binary adducts comprising two different cyclic...
2.
Islam S, Yasmeen R, Verma G, Tekarli S, Nesterov V, Ma S, et al.
Inorg Chem . 2024 May; 63(19):8664-8673. PMID: 38696593
C2 hydrocarbon separation from methane represents a technological challenge for natural gas upgrading. Herein, we report a new metal-organic framework, [CuL(DEF)]·2DEF (; HL = 4,4',4″,4‴-((1,1',1″,1‴)-benzene-1,2,4,5-tetrayltetrakis(ethene-2,1-diyl))tetrabenzoic acid; DEF = ,-diethylformamide; UNT...
3.
Cooper C, Paul R, Alsaleh A, Washburn S, Rackers W, Kumar S, et al.
Chemistry . 2023 Jul; 29(57):e202302013. PMID: 37467466
The fusion of tetrapyrroles with aromatic heterocycles constitutes a useful tool for manipulating their opto-electronic properties. In this work, the synthesis of naphthodithiophene-fused porphyrins was achieved through a Heck reaction-based...
4.
Holzer N, Jin J, Nesterov V, Sharma J, Zarrabi N, DSouza F, et al.
Inorg Chem . 2023 Apr; 62(18):7097-7110. PMID: 37099270
A series of fluorinated antimony(V) porphyrins, SbTPP(OMe)·PF, SbTPP(OTFE)·PF, SbT(4F)PP(OMe)·PF, SbT(35F)PP(OMe)·PF, SbT(345F)PP(OMe)·PF, SbT(4CF)PP(OMe)·PF, SbT(35CF)PP(OMe)·PF, and SbT(35CF)PP(OTFE)·PF, have been synthesized with phenyl [P], 4-fluorophenyl [(4F)P], 3,5-difluorophenyl [(35F)P], 3,4,5-difluorophenyl [(345F)P], 4-trifluoromethylphenyl [(4CF)P], and...
5.
Moss A, Nevonen D, Hu Y, Nesterov V, Nemykin V, Wang H
ACS Phys Chem Au . 2023 Mar; 2(6):468-481. PMID: 36855607
Unsymmetric pentacenequinone-fused (cross-conjugated) and pentacene-fused (linear-conjugated) porphyrins were designed and synthesized. The cross-conjugated ( - ) and linear-conjugated ( - ) porphyrins displayed strikingly different sets of optical and electronic...
6.
Cortes Vazquez J, Alharbi W, Davis J, Moore A, Nesterov V, Cundari T, et al.
ACS Omega . 2022 Dec; 7(49):45341-45346. PMID: 36530259
A three-component cascade reaction comprising cyclic ketones, arylamines, and benzoylmethylene malonates has been developed to access 4,5,6,7-tetrahydro-1-indoles. The reaction was achieved through cooperative enamine-Brønsted catalysis in high yields with wide...
7.
Welton C, Nesterov V, Smucker B
IUCrdata . 2022 Nov; 7(Pt 3):x220248. PMID: 36339800
Crystals of the title compound, CHN ·BF , were unexpectedly grown from crystallization attempts of [Pt(4,4'-bpy)](BF) [Smith (2019 ▸). , 188-215] using toluene and aceto-nitrile. The tetra-fluoro-borate anion and the...
8.
Sharma J, Bayard B, Zosel N, Ali S, Holzer N, Nesterov V, et al.
Inorg Chem . 2022 Oct; 61(42):16573-16585. PMID: 36223643
To study the photophysical and redox properties as a function of -aryl units, a series of hypervalent phosphorus(V) porphyrins, PP(OMe)·PF, PMP(OMe)·PF, PDMP(OMe)·PF, P345TMP(OMe)·PF, and P246TMP(OMe)·PF, with phenyl (P), 4-methoxyphenyl (MP),...
9.
Moss A, Jang Y, Arvidson J, Nesterov V, DSouza F, Wang H
Chem Sci . 2022 Oct; 13(34):9880-9890. PMID: 36199634
A new synthetic method to fuse benzo[4,5]imidazo[2,1-]isoindole to the porphyrin periphery at the β,β-positions has been developed, and its impact on the aromaticity and electronic structures is investigated. Reactivity investigation...
10.
Getmanenko Y, Mullins C, Nesterov V, Lake S, Risko C, Johnston-Halperin E
RSC Adv . 2022 May; 8(63):36223-36232. PMID: 35558484
Here we present the synthesis and characterization of a hybrid vanadium-organic coordination polymer with robust magnetic order, a Curie temperature of ∼110 K, a coercive field of ∼5 Oe at...