Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Gonzalo Anguera"'
Publikováno v:
Journal of Porphyrins and Phthalocyanines. 24:350-354
Mesoporous silica nanoparticles decorated with 2,7,12,17-tetraphenylporphycene have been prepared by reaction of aminated nanoparticles with 9-(glutaric [Formula: see text]-succinimidylesteramide)-2,7,12,17-tetraphenylporphycene. The as-prepared nano
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df03a5b31ff63cc206d47ec3d84f099a
https://doi.org/10.1142/s1088424619500986
https://doi.org/10.1142/s1088424619500986
Publikováno v:
Synlett. 30:765-769
Porphycenes, the first structural isomer of porphyrin, display unique chemical and photophysical properties. In this Account, we detail our group’s individual and collaborative efforts in elucidating further the chemical properties of porphycene. P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66c5c9bf6dda1dbf60cc9dcdfe3ccd55
https://doi.org/10.1055/s-0037-1610345
https://doi.org/10.1055/s-0037-1610345
Autor:
Hadiqa Zafar, James T. Brewster, Gonzalo Anguera, Matthew D. Moore, Apolonio Aguilar, Jonathan L. Sessler
Publikováno v:
Journal of Coordination Chemistry. 71:1808-1813
The reaction between amethyrin and non-aqueous uranyl silylamide (UO2[N(SiMe3)2]2) under anaerobic conditions affords a bench-stable uranyl complex. UV–vis spectroscopy, cyclic voltammetry, as well as proton NMR spectroscopic analyses provide suppo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b6ca228845a4ea909e299142e3e2e37
https://doi.org/10.1080/00958972.2018.1458230
https://doi.org/10.1080/00958972.2018.1458230
Autor:
Dongho Kim, Matthew D. Moore, Won Young Cha, Ju-Hoon Lee, Vincent M. Lynch, Jonathan L. Sessler, Shenyi Guo, Gonzalo Anguera
Publikováno v:
Journal of the American Chemical Society. 140:4028-4034
A new expanded porphyrin, hexadecaphyrin-(1.0.0.0.1.1.0.1.1.0.0.0.1.1.0.1), is reported. It was obtained via the condensation of a hexapyrrolic derivative prepared in turn from a bipyrrole dialdehyde and a stable quaterpyrrole precursor. This hexadec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc5532832caaee31390bd7e16f2f49e2
https://doi.org/10.1021/jacs.7b13024
https://doi.org/10.1021/jacs.7b13024
Autor:
Gonzalo Anguera, James T. Brewster, Dongho Kim, Vincent D. Lynch, Jonathan L. Sessler, Matthew D. Moore, Won Young Cha, Michael Y. Zhao
Publikováno v:
Angewandte Chemie International Edition. 57:2575-2579
A new expanded porphycene with 26 π-electrons has been prepared by the McMurry coupling of 1,4-bis(3,4-diethyl-2-pyrryl)benzene dialdehyde. Expansion of the porphycene framework provides a ligand capable of stabilizing a bis(rhodium) and a monoruthe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72e8acd4d8c87bf00f88cc1b0ab60c4f
https://doi.org/10.1002/anie.201711197
https://doi.org/10.1002/anie.201711197
Publikováno v:
Macroheterocycles. 11:227-245
Functionalized N-unsubstituted 2,2’-bipyrroles are basic building blocks for the preparation of pyrrolic macrocycles and natural products, such as prodigiosines. The aim of this review is to provide a description of the most important methodologies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74cb96e73eb618540ac228548c788140
https://doi.org/10.6060/mhc180483s
https://doi.org/10.6060/mhc180483s
Autor:
Gonzalo Anguera, Matthew D. Moore, Ju-Hoon Lee, Vincent M. Lynch, Jonathan L. Sessler, Gabriela I. Vargas-Zúñiga, Hadiqa Zafar, James T. Brewster
Publikováno v:
Inorganic Chemistry. 56:9409-9412
Using naphthobipyrrole as a functional building block, a new expanded porphyrin, naphthoisoamethyrin, was prepared in 85% yield under acid-catalyzed [4 + 2] MacDonald coupling conditions. Treatment of naphthoisoamethyrin with the nonaqueous uranyl si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b73ee05d8a79f000a9aabd5104de5ed1
https://doi.org/10.1021/acs.inorgchem.7b01668
https://doi.org/10.1021/acs.inorgchem.7b01668
Publikováno v:
The Journal of Organic Chemistry. 82:6904-6912
The preparation and characterization of a family of stable 2,2′-bipyrroles substituted at positions 5 and 5′ with thienyl, phenyl, TMS-ethynyl, and vinyl groups is reported herein. The synthesis of these new bipyrroles comprises three steps: form
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b36ec6f2914317b002f3c66460177ed4
https://doi.org/10.1021/acs.joc.7b00961
https://doi.org/10.1021/acs.joc.7b00961
Autor:
David Sánchez-García, Gonzalo Anguera
Publikováno v:
Chemical Reviews. 117:2481-2516
Porphyrins, called the pigments of life, have been studied for decades. However, the first constitutional isomer of porphyrin, porphycene, was not synthesized until 1986. This milestone marked the beginning of a new era in the field of porphyrinoids
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e46839b653f7d7132f435205ee625402
https://doi.org/10.1021/acs.chemrev.6b00345
https://doi.org/10.1021/acs.chemrev.6b00345
Autor:
Gonzalo Anguera, Christopher D. Wight, Vincent M. Lynch, Hadiqa Zafar, James T. Brewster, Axel Steinbrück, Matthew McVeigh, Jonathan L. Sessler
Publikováno v:
The Journal of Organic Chemistry. 83:9568-9570
The controlled preparation of higher order oligopyr-rolic species holds broad utility across the chemical and material sciences. Here, we describe the gram-scale synthesis of a bench-stable 5,5”-unsubstituted terpyrrole in excellent yield via a tan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92c0a36d238917d1a8144987d7af8a3e
https://doi.org/10.1021/acs.joc.8b01333
https://doi.org/10.1021/acs.joc.8b01333