Every reference with a DOI in the deposited reference list resolved to a known
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The 44 checked references that resolve
resolves10.1039/cs9952400019Photosensitizers of the porphyrin and phthalocyanine series for photodynamic therapy
resolves10.1021/ja991730dTemplate-Directed Synthesis, Excited-State Photodynamics, and Electronic Communication in a Hexameric Wheel of Porphyrins
resolves10.1021/jo302135qTetraaryltetraanthra[2,3]porphyrins: Synthesis, Structure, and Optical Properties
resolves10.1021/ja0445847Understanding Strong Two-Photon Absorption in π-Conjugated Porphyrin Dimers via Double-Resonance Enhancement in a Three-Level Model
resolves10.1021/jp020398gUltrafast Dynamics of Porphyrins in the Condensed Phase: I. Free Base Tetraphenylporphyrin
resolves10.1038/nmat2986Porphysome nanovesicles generated by porphyrin bilayers for use as multimodal biophotonic contrast agents
resolves10.1039/a902802aRecent development in the design of organic materials for optical power limiting
resolves10.1021/jp304817uModeling of Nonlinear Absorption of 5,10-A<sub>2</sub>B<sub>2</sub>Porphyrins in the Nanosecond Regime
resolves10.1039/c3pp25410kNonlinear absorption properties of 5,10-A2B2porphyrins—correlation of molecular structure with the nonlinear responses
resolves10.1039/c3pp50156fSolvent effect on the nonlinear absorption of 5,10-A2B2meso substituted porphyrins
resolves10.1039/C4PP00435CHow green is green chemistry? Chlorophylls as a bioresource from biorefineries and their commercial potential in medicine and photovoltaics
resolves10.1002/mabi.201300149Triplet–<scp>T</scp>riplet Annihilation Upconversion Based Nanocapsules for Bioimaging Under Excitation by Red and Deep‐<scp>R</scp>ed Light
resolves10.1016/j.saa.2013.04.065Effect of interaction with micelles on the excited-state optical properties of zinc porphyrins and J-aggregates formation
resolves10.1021/jp205963kInvestigation of Ground- and Excited-State Photophysical Properties of 5,10,15,20-Tetra(4-pyridyl)-21H,23H-porphyrin with Ruthenium Outlying Complexes
resolves10.1002/ejoc.2011006415,15‐A<sub>2</sub>B<sub>2</sub>‐ and 5,15‐A<sub>2</sub>BC‐Type Porphyrins with Donor and Acceptor Groups for Use in Nonlinear Optics and Photodynamic Therapy
resolves10.1016/j.tet.2005.03.086Lead structures for applications in photodynamic therapy. Part 1: Synthesis and variation of m-THPC (Temoporfin) related amphiphilic A2BC-type porphyrins
resolves10.1016/j.cplett.2009.06.089Correlation studies on structurally diverse porphyrin monomers, dimers and trimers and their nonlinear optical responses
resolves10.1021/jm800125aImprovement of<i>meta</i>-tetra(Hydroxyphenyl)chlorin-Like Photosensitizer Selectivity with Folate-Based Targeted Delivery. Synthesis and in Vivo Delivery Studies
resolves10.1002/ejoc.200901113Synthesis of <i>meso</i>‐Substituted ABCD‐Type Porphyrins by Functionalization Reactions
resolves10.1039/B618996BA
<sub>2</sub>
B
<sub>2</sub>
-type push–pull porphyrins as reverse saturable and saturable absorbers
resolves10.1002/jpp.389Hydrophilicity vs hydrophobicity — varying the amphiphilic structure of porphyrins related to the photosensitizer m-THPC
resolves10.1002/chem.2011019345,10‐A<sub>2</sub>B<sub>2</sub>‐Type <i>meso</i>‐Substituted Porphyrins—A Unique Class of Porphyrins with a Realigned Dipole Moment
resolves10.1351/PAC-REP-10-09-31Standards for photoluminescence quantum yield measurements in solution (IUPAC Technical Report)
resolves10.1016/S0022-2860(01)00870-5Substitution effect of hydroxyl group on photophysical properties of tetraphenylporphyrin (H 2 TPP) and germanium(IV) tetraphenylporphyrin dichloride (Ge(IV)TPPCl 2 )
resolves10.1021/ja038676sDesign, Synthesis, and Photophysical Studies of a Porphyrin-Fullerene Dyad with Parachute Topology; Charge Recombination in the Marcus Inverted Region
resolves10.1021/j100129a017Spectroscopic, photophysical, and redox properties of some meso-substituted free-base porphyrins
resolves10.1021/ja00851a015Luminescence studies on several tetraarylporphins and their zinc derivatives
resolves10.1039/f19807601978Luminescence of porphyrins and metalloporphyrins. Part 1.—Zinc(II), nickel(II) and manganese(II) porphyrins
resolves10.1038/srep04447Molecular Structure – Optical Property Relationships for a Series of Non-Centrosymmetric Two-photon Absorbing Push-Pull Triarylamine Molecules
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