Research graph
References from Improving the photodynamic activity of metallochlorins by combined computational design and experimental validation. Local targets link to admitted publications; unresolved targets remain external evidence.
Introduction to cancer and Treatment Approaches
2022 · External reference
Updating the definition of Cancer
10.1158/1541-7786.mcr-23-0411 · 2023 · External reference
Accessories to the crime: functions of cells recruited to the tumor microenvironment
10.1016/j.ccr.2012.02.022 · 2012 · External reference
Cancer statistics, 2026
2026 · External reference
Advancements and limitations in traditional anti-cancer therapies: a comprehensive review of surgery, chemotherapy, radiation therapy, and hormonal therapy
10.1007/s12672-025-02198-8 · 2025 · External reference
Chemotherapy side-effects: not all DNA damage is equal
10.3390/cancers14030627 · 2022 · External reference
10.2147/ijn.s584604
10.2147/ijn.s584604 · External reference
Nanoparticle-based drug delivery systems targeting cancer cell surfaces
10.1039/d3ra02969g · 2023 · External reference
Engineering combination nanomedicines to overcome cancer resistance
10.1039/d5ra08728g · 2026 · External reference
Recent progress in photosensitizers for overcoming the challenges of photodynamic therapy: from molecular design to application
10.1039/d0cs00173b · 2021 · External reference
Recent advances for enhanced photodynamic therapy: from new mechanisms to innovative strategies
10.1039/d3sc07006a · 2024 · External reference
Mechanisms in photodynamic therapy: part one—photosensitizers, photochemistry and cellular localization
10.1016/s1572-1000(05)00007-4 · 2004 · External reference
Spin–orbit coupling and intersystem crossing in molecules, WIREs computational molecular
2012 · External reference
Synthesis and characterization of photodynamic activity of an iodinated chlorin e6 copper complex
10.1039/c6ra14026b · 2016 · External reference
Synergistic effects of metals in a promising Ru (II)−pt(II) assembly for a combined anticancer approach: theoretical exploration of the photophysical properties, chemistry – a
10.1002/chem.201601089 · 2016 · External reference
Tuning the photophysical properties of Ru(II) photosensitizers for PDT by protonation and Metallation: a DFT study
10.1021/acs.jpca.3c00839 · 2023 · External reference
Porphyrin photosensitizer molecules as effective medicine candidates for photodynamic therapy: electronic structure information aided design
10.1039/d4ra05585c · 2024 · External reference
Aromatic pathways of porphins, chlorins, and Bacteriochlorins
10.1021/jo300182b · 2012 · External reference
Photodynamic therapy, priming and optical imaging: potential co-conspirators in treatment design and optimization — a Thomas Dougherty award for excellence in PDT paper
10.1142/s1088424620300098 · 2020 · External reference
Exploring the spectral properties and potential applications of dimethylamine-modified porphyrin and chlorin dyes
10.1016/j.jphotochem.2024.115742 · 2024 · External reference
Synthesis of locked meso-β-substituted chlorins via 1,3-dipolar cycloaddition
10.1021/jo060545x · 2006 · External reference
Long-wavelength absorbing Benzimidazolo-chlorin for enhanced photodynamic therapy
10.1021/acsomega.3c01807 · 2023 · External reference
Photodynamic therapy for cancer: mechanisms, photosensitizers, nanocarriers, and clinical studies
2024 · External reference
In vitro heavy-atom effect of palladium(II) and platinum(II) complexes of pyrrolidine-fused chlorin in photodynamic therapy
10.1021/jm8015427 · 2009 · External reference
Nanoparticles in photodynamic therapy
10.1021/cr5004198 · 2015 · External reference
Enhancement of the triplet photosensitizing ability of BODIPY dyes by controlled red-shifted H-aggregate formation using ionic liquids: insights from spectroscopy, microscopy, DFT and biological studies
10.1039/d5cp01890k · 2025 · External reference
Application of TD-DFT theory to studying Porphyrinoid-based photosensitizers for photodynamic therapy: a review
10.3390/molecules26237176 · 2021 · External reference
Calculation of potential energy surfaces with quantum Monte Carlo as a useful tool for the design of green chemical syntheses: The HOCO radical test case
2022 · External reference
Ohmic heating-assisted synthesis and characterization of Zn(ii), cu(ii) and pd(ii) complexes of heterocyclic-fused chlorins
10.1039/d1dt04032d · 2022 · External reference
Some new aspects related to the synthesis of meso-substituted porphyrins
10.1002/jhet.5570280317 · 1991 · External reference
1,3-dipolar cycloaddition reactions of porphyrins with azomethine ylides
10.1021/jo048349i · 2005 · External reference
Synthesis of non-aggregating chlorins and isobacteriochlorins from meso-tetrakis(pentafluorophenyl)porphyrin: a study using 1,3-dipolar cycloadditions under mild conditions
10.1016/j.tetlet.2014.01.049 · 2014 · External reference
Coordination-induced spin-state switching with nickel chlorin and nickel isobacteriochlorin
10.1021/acs.inorgchem.5b01756 · 2015 · External reference
A parahydrogen based NMR study of pt catalysed alkyne hydrogenation
10.1039/b925196k · 2010 · External reference
Quantum yields for the photosensitized formation of the lowest electronically excited singlet state of molecular oxygen in solution
10.1063/1.555934 · 1993 · External reference
A new local density functional for main-group thermochemistry, transition metal bonding, thermochemical kinetics, and noncovalent interactions
10.1063/1.2370993 · 2006 · External reference
10.1007/s00214-007-0310-x
10.1007/s00214-007-0310-x · 2008 · External reference
Self-consistent molecular orbital methods. XX. A basis set for correlated wave functions
10.1063/1.438955 · 1980 · External reference
Energy-adjustedab initio pseudopotentials for the second and third row transition elements
10.1007/bf01114537 · 1990 · External reference
Unresolved reference
2019 · External reference
Quantum mechanical continuum solvation models
10.1021/cr9904009 · 2005 · External reference
The ORCA program system
10.1002/wcms.81 · 2012 · External reference
The zero-order regular approximation for relativistic effects: the effect of spin–orbit coupling in closed shell molecules
10.1063/1.472460 · 1996 · External reference
Density-functional thermochemistry. III. The role of exact exchange
10.1063/1.464913 · 1993 · External reference
Dynamic correlation
10.1080/00268970010023435 · 2001 · External reference
A new hybrid exchange–correlation functional using the coulomb-attenuating method (CAM-B3LYP)
10.1016/j.cplett.2004.06.011 · 2004 · External reference
Long-range corrected hybrid density functionals with damped atom–atom dispersion corrections
10.1039/b810189b · 2008 · External reference
Isoxazolidine-fused meso-tetraarylchlorins as key tools for the synthesis of mono- and bis-annulated chlorins
10.1039/c5ob00800j · 2015 · External reference
Exploring the effect of porphyrin chemical structure on the performance of polymer-based pressure-sensitive paints
10.1016/j.snb.2024.135577 · 2024 · External reference
Transition metal complexes and photodynamic therapy from a tumor-Centered approach: challenges, opportunities, and highlights from the development of TLD1433
10.1021/acs.chemrev.8b00211 · 2019 · External reference
Time-resolved EPR, fluorescence, and transient absorption studies on Phthalocyaninatosilicon covalently linked to one or two TEMPO radicals
10.1021/ja002780h · 2001 · External reference
Photosensitization mechanism of cu(ii) porphyrins
10.1039/c7cp03319b · 2017 · External reference
The role of molecular oxygen in the photodynamic effect of phthalocyanines
10.2307/3576857 · 1986 · External reference
Structural aspects of porphyrins for functional materials applications
10.3390/cryst7070223 · 2017 · External reference
Porphyrin metalation catalyzed by DNAzymes and nanozymes
10.1039/d1qi00105a · 2021 · External reference
New conjugatable platinum(II) chlorins: synthesis, reactivity and singlet oxygen generation
10.3390/molecules30122496 · 2025 · External reference
Dinuclear ruthenium(II)-Pyrrolide complexes linked by different organic units as PDT photosensitizers: computational study of the linker influence on the photophysical properties*
10.1002/cptc.202200094 · 2022 · External reference
Tuning the singlet-triplet energy gap: a unique approach to efficient photosensitizers with aggregation-induced emission (AIE) characteristics
10.1039/c5sc01733e · 2015 · External reference
Heat and mass transfer, basic principles
2018 · External reference
Photophysical origin of the reduced photodynamic therapy activity of temocene compared to Foscan®: insights from theory
10.1039/c3cp52698d · 2013 · External reference
Predictive power of long-range corrected functionals on the spectroscopic properties of tetrapyrrole derivatives for photodynamic therapy
10.1039/c0cp02792h · 2011 · External reference
Excited-state absorption in tetrapyridyl porphyrins: comparing real-time and quadratic-response time-dependent density functional theory
10.1039/c7cp04567k · 2017 · External reference
Theoretical UV-vis spectra of tetracationic porphyrin: effects of environment on electronic spectral properties
10.1007/s00894-019-4149-6 · 2019 · External reference
Photophysical properties of 1,3-Diphenylisobenzofuran as a sensitizer and its reaction with O2
10.3390/molecules30143021 · 2025 · External reference
Singlet oxygen quantum yield determination using chemical acceptors
10.1007/978-1-0716-0896-8_14 · 2021 · External reference
Methylene blue in anticancer photodynamic therapy: systematic review of preclinical studies
10.3389/fphar.2023.1264961 · 2023 · External reference
Singlet oxygen quantum yields of potential porphyrin-based photosensitisers for photodynamic therapy
10.1039/b705853e · 2007 · External reference
Singlet oxygen production by a polypyridine ruthenium (II) complex with a perylene monoimide derivative: a strategy for photodynamic inactivation of Candida albicans
10.1016/j.jphotochem.2017.12.020 · 2018 · External reference
Synergistic effects of metals in a promising Ru (II)−pt(II) assembly for a combined anticancer approach: theoretical exploration of the photophysical properties, chemistry – a
10.1002/chem.201601089 · ExternalCitation · doi-reference
Dinuclear ruthenium(II)-Pyrrolide complexes linked by different organic units as PDT photosensitizers: computational study of the linker influence on the photophysical properties*
10.1002/cptc.202200094 · ExternalCitation · doi-reference
Some new aspects related to the synthesis of meso-substituted porphyrins
10.1002/jhet.5570280317 · ExternalCitation · doi-reference
The ORCA program system
10.1002/wcms.81 · ExternalCitation · doi-reference
Singlet oxygen quantum yield determination using chemical acceptors
10.1007/978-1-0716-0896-8_14 · ExternalCitation · doi-reference
Energy-adjustedab initio pseudopotentials for the second and third row transition elements
10.1007/bf01114537 · ExternalCitation · doi-reference
10.1007/s00214-007-0310-x
10.1007/s00214-007-0310-x · ExternalCitation · doi-reference
Theoretical UV-vis spectra of tetracationic porphyrin: effects of environment on electronic spectral properties
10.1007/s00894-019-4149-6 · ExternalCitation · doi-reference
Advancements and limitations in traditional anti-cancer therapies: a comprehensive review of surgery, chemotherapy, radiation therapy, and hormonal therapy
10.1007/s12672-025-02198-8 · ExternalCitation · doi-reference
Accessories to the crime: functions of cells recruited to the tumor microenvironment
10.1016/j.ccr.2012.02.022 · ExternalCitation · doi-reference
A new hybrid exchange–correlation functional using the coulomb-attenuating method (CAM-B3LYP)
10.1016/j.cplett.2004.06.011 · ExternalCitation · doi-reference
Singlet oxygen production by a polypyridine ruthenium (II) complex with a perylene monoimide derivative: a strategy for photodynamic inactivation of Candida albicans
10.1016/j.jphotochem.2017.12.020 · ExternalCitation · doi-reference
Exploring the spectral properties and potential applications of dimethylamine-modified porphyrin and chlorin dyes
10.1016/j.jphotochem.2024.115742 · ExternalCitation · doi-reference
Exploring the effect of porphyrin chemical structure on the performance of polymer-based pressure-sensitive paints
10.1016/j.snb.2024.135577 · ExternalCitation · doi-reference
Synthesis of non-aggregating chlorins and isobacteriochlorins from meso-tetrakis(pentafluorophenyl)porphyrin: a study using 1,3-dipolar cycloadditions under mild conditions
10.1016/j.tetlet.2014.01.049 · ExternalCitation · doi-reference
Mechanisms in photodynamic therapy: part one—photosensitizers, photochemistry and cellular localization
10.1016/s1572-1000(05)00007-4 · ExternalCitation · doi-reference
Transition metal complexes and photodynamic therapy from a tumor-Centered approach: challenges, opportunities, and highlights from the development of TLD1433
10.1021/acs.chemrev.8b00211 · ExternalCitation · doi-reference
Coordination-induced spin-state switching with nickel chlorin and nickel isobacteriochlorin
10.1021/acs.inorgchem.5b01756 · ExternalCitation · doi-reference
Tuning the photophysical properties of Ru(II) photosensitizers for PDT by protonation and Metallation: a DFT study
10.1021/acs.jpca.3c00839 · ExternalCitation · doi-reference
Long-wavelength absorbing Benzimidazolo-chlorin for enhanced photodynamic therapy
10.1021/acsomega.3c01807 · ExternalCitation · doi-reference
Nanoparticles in photodynamic therapy
10.1021/cr5004198 · ExternalCitation · doi-reference
Quantum mechanical continuum solvation models
10.1021/cr9904009 · ExternalCitation · doi-reference
Time-resolved EPR, fluorescence, and transient absorption studies on Phthalocyaninatosilicon covalently linked to one or two TEMPO radicals
10.1021/ja002780h · ExternalCitation · doi-reference
In vitro heavy-atom effect of palladium(II) and platinum(II) complexes of pyrrolidine-fused chlorin in photodynamic therapy
10.1021/jm8015427 · ExternalCitation · doi-reference
1,3-dipolar cycloaddition reactions of porphyrins with azomethine ylides
10.1021/jo048349i · ExternalCitation · doi-reference
Synthesis of locked meso-β-substituted chlorins via 1,3-dipolar cycloaddition
10.1021/jo060545x · ExternalCitation · doi-reference
Aromatic pathways of porphins, chlorins, and Bacteriochlorins
10.1021/jo300182b · ExternalCitation · doi-reference
Singlet oxygen quantum yields of potential porphyrin-based photosensitisers for photodynamic therapy
10.1039/b705853e · ExternalCitation · doi-reference
Long-range corrected hybrid density functionals with damped atom–atom dispersion corrections
10.1039/b810189b · ExternalCitation · doi-reference
A parahydrogen based NMR study of pt catalysed alkyne hydrogenation
10.1039/b925196k · ExternalCitation · doi-reference
Predictive power of long-range corrected functionals on the spectroscopic properties of tetrapyrrole derivatives for photodynamic therapy
10.1039/c0cp02792h · ExternalCitation · doi-reference
Photophysical origin of the reduced photodynamic therapy activity of temocene compared to Foscan®: insights from theory
10.1039/c3cp52698d · ExternalCitation · doi-reference
Isoxazolidine-fused meso-tetraarylchlorins as key tools for the synthesis of mono- and bis-annulated chlorins
10.1039/c5ob00800j · ExternalCitation · doi-reference
Tuning the singlet-triplet energy gap: a unique approach to efficient photosensitizers with aggregation-induced emission (AIE) characteristics
10.1039/c5sc01733e · ExternalCitation · doi-reference
Synthesis and characterization of photodynamic activity of an iodinated chlorin e6 copper complex
10.1039/c6ra14026b · ExternalCitation · doi-reference
Photosensitization mechanism of cu(ii) porphyrins
10.1039/c7cp03319b · ExternalCitation · doi-reference
Excited-state absorption in tetrapyridyl porphyrins: comparing real-time and quadratic-response time-dependent density functional theory
10.1039/c7cp04567k · ExternalCitation · doi-reference
Recent progress in photosensitizers for overcoming the challenges of photodynamic therapy: from molecular design to application
10.1039/d0cs00173b · ExternalCitation · doi-reference
Ohmic heating-assisted synthesis and characterization of Zn(ii), cu(ii) and pd(ii) complexes of heterocyclic-fused chlorins
10.1039/d1dt04032d · ExternalCitation · doi-reference
Porphyrin metalation catalyzed by DNAzymes and nanozymes
10.1039/d1qi00105a · ExternalCitation · doi-reference
Nanoparticle-based drug delivery systems targeting cancer cell surfaces
10.1039/d3ra02969g · ExternalCitation · doi-reference
Recent advances for enhanced photodynamic therapy: from new mechanisms to innovative strategies
10.1039/d3sc07006a · ExternalCitation · doi-reference
Porphyrin photosensitizer molecules as effective medicine candidates for photodynamic therapy: electronic structure information aided design
10.1039/d4ra05585c · ExternalCitation · doi-reference
Enhancement of the triplet photosensitizing ability of BODIPY dyes by controlled red-shifted H-aggregate formation using ionic liquids: insights from spectroscopy, microscopy, DFT and biological studies
10.1039/d5cp01890k · ExternalCitation · doi-reference
Engineering combination nanomedicines to overcome cancer resistance
10.1039/d5ra08728g · ExternalCitation · doi-reference
A new local density functional for main-group thermochemistry, transition metal bonding, thermochemical kinetics, and noncovalent interactions
10.1063/1.2370993 · ExternalCitation · doi-reference
Self-consistent molecular orbital methods. XX. A basis set for correlated wave functions
10.1063/1.438955 · ExternalCitation · doi-reference
Density-functional thermochemistry. III. The role of exact exchange
10.1063/1.464913 · ExternalCitation · doi-reference
The zero-order regular approximation for relativistic effects: the effect of spin–orbit coupling in closed shell molecules
10.1063/1.472460 · ExternalCitation · doi-reference
Quantum yields for the photosensitized formation of the lowest electronically excited singlet state of molecular oxygen in solution
10.1063/1.555934 · ExternalCitation · doi-reference
Dynamic correlation
10.1080/00268970010023435 · ExternalCitation · doi-reference
Photodynamic therapy, priming and optical imaging: potential co-conspirators in treatment design and optimization — a Thomas Dougherty award for excellence in PDT paper
10.1142/s1088424620300098 · ExternalCitation · doi-reference
Updating the definition of Cancer
10.1158/1541-7786.mcr-23-0411 · ExternalCitation · doi-reference
10.2147/ijn.s584604
10.2147/ijn.s584604 · ExternalCitation · doi-reference
The role of molecular oxygen in the photodynamic effect of phthalocyanines
10.2307/3576857 · ExternalCitation · doi-reference
Methylene blue in anticancer photodynamic therapy: systematic review of preclinical studies
10.3389/fphar.2023.1264961 · ExternalCitation · doi-reference
Chemotherapy side-effects: not all DNA damage is equal
10.3390/cancers14030627 · ExternalCitation · doi-reference
Structural aspects of porphyrins for functional materials applications
10.3390/cryst7070223 · ExternalCitation · doi-reference
Application of TD-DFT theory to studying Porphyrinoid-based photosensitizers for photodynamic therapy: a review
10.3390/molecules26237176 · ExternalCitation · doi-reference
New conjugatable platinum(II) chlorins: synthesis, reactivity and singlet oxygen generation
10.3390/molecules30122496 · ExternalCitation · doi-reference
Photophysical properties of 1,3-Diphenylisobenzofuran as a sensitizer and its reaction with O2
10.3390/molecules30143021 · ExternalCitation · doi-reference
