Chiroptical properties of cyanine aggregates: hierarchical modelling from monomers to bundles.

Some achiral cyanine dyes form well-ordered chiral assemblies exhibiting pronounced Circular Dichroism (CD) and Circularly Polarized Luminescence (CPL). Notably, achiral C8O3 cyanines self-assemble into tubular J-aggregates, which further organize into bundles displaying bisignate CD spectrum - hallmark of an exciton coupled system - and an unusual bisignated CPL. In contrast, the tubular aggregates display a monosignate CD spectrum.

Shedding light on thermally-activated delayed fluorescence.

Thermally activated delayed fluorescence (TADF) is a hot research topic in view of its impressive applications in a wide variety of fields from organic LEDs to photodynamic therapy and metal-free photocatalysis. TADF is a rare and fragile phenomenon that requires a delicate equilibrium between tiny singlet-triplet gaps, sizable spin-orbit couplings, conformational flexibility and a balanced contribution of charge transfer and local excited states. To make the picture more complex, this precarious equilibrium is non-trivially affected by the interaction of the TADF dye with its local environment.

Shining Light on Inverted Singlet-Triplet Emitters.

The inversion of the lowest singlet and triplet excited states, observed in several triangle-shaped organic molecules containing conjugated carbon and nitrogen atoms, is an astonishing result that implies the breakdown of Hund's rule. The phenomenon attracted interest for its potential toward triplet harvesting in organic LEDs. On a more fundamental vein, the singlet-triplet (ST) inversion sheds new light on the role of electron correlations in the excited-state landscape of π-conjugated molecules.

Solid state solvation: a fresh view.

The design of efficient organic electronic devices, including OLEDs, OPVs, luminescent solar concentrators, , relies on the optimization of relevant materials, often constituted by an active (functional) dye embedded in a matrix. Understanding solid state solvation (SSS), how the properties of the active dye are affected by the matrix, is therefore an issue of fundamental and technological relevance. Here an extensive experimental and theoretical investigation is presented shedding light on this, somewhat controversial, topic.

Aggregates of Cyanine Dyes: When Molecular Vibrations and Electrostatic Screening Make the Difference.

Aggregates of cyanine dyes are currently investigated as promising materials for advanced electronic and photonic applications. The spectral properties of aggregates of cyanine dyes can be tuned by altering the supramolecular packing, which is affected by the length of the dye, the presence of alkyl chains, or the nature of the counterions. In this work, we present a joint experimental and theoretical study of a family of cyanine dyes forming aggregates of different types according to the length of the polymethinic chain.

Novel Method for the Synthesis of Merocyanines: New Photophysical Possibilities for a Known Class of Fluorophores.

A new, transformative method for the preparation of rhodols and other merocyanines from readily available tetrafluorohydroxybenzaldehyde and aminophenols has been developed. It is now possible to prepare merocyanines bearing three fluorine atoms and additional conjugated rings, and the whole one-pot process occurs under neutral, mild conditions. Three heretofore unknown merocyanine-based architectures were prepared using this strategy from aminonaphthols and 4-hydroxycoumarins.

Circular dichroism of molecular aggregates: A tutorial.

In this tutorial, we guide the reader through two alternative approaches to the calculation of circular dichroism (CD) spectra of chiral supramolecular assemblies of non-chiral chromophores. The two seemingly different approaches rely on the same basic approximations and are therefore expected to lead to similar results. For a dimer, we obtain explicit analytic expressions for the CD responses in the two approaches and demonstrate the perfect equivalence of the two methods.

From symmetry breaking to symmetry swapping: is Kasha's rule violated in multibranched phenyleneethynylenes?

The phenomenon of excited-state symmetry breaking is often observed in multipolar molecular systems, significantly affecting their photophysical and charge separation behavior. As a result of this phenomenon, the electronic excitation is partially localized in one of the molecular branches. However, the intrinsic structural and electronic factors that regulate excited-state symmetry breaking in multibranched systems have hardly been investigated.

Ultrabright Föster Resonance Energy Transfer Nanovesicles: The Role of Dye Diffusion.

The development of contrast agents based on fluorescent nanoparticles with high brightness and stability is a key factor to improve the resolution and signal-to-noise ratio of current fluorescence imaging techniques. However, the design of bright fluorescent nanoparticles remains challenging due to fluorescence self-quenching at high concentrations. Developing bright nanoparticles showing FRET emission adds several advantages to the system, including an amplified Stokes shift, the possibility of ratiometric measurements, and of verifying the nanoparticle stability.

Thermally Activated Delayed Fluorescence: Polarity, Rigidity, and Disorder in Condensed Phases.

We present a detailed and comprehensive picture of the photophysics of thermally activated delayed fluorescence (TADF). The approach relies on a few-state model, parametrized on a prototypical TADF dye, that explicitly accounts for the nonadiabatic coupling between electrons and vibrational and conformational motion, crucial to properly address (reverse) intersystem crossing rates. The Onsager model is exploited to account for the medium polarity and polarizability, with careful consideration of the different time scales of relevant degrees of freedom.

Mean-Field Effects on the Phosphorescence of Dinuclear Re(I) Complex Polymorphs.

A computational study rationalizes the different phosphorescence colors of two highly emitting crystal polymorphs of a dinuclear Re(I) complex, [Re(μ-Cl)(CO)(μ-4,5-(MeSi)pyridazine)]. The electrostatic interactions between the charge distributions on neighboring molecules inside the crystal are responsible for the different stabilization of the emitting triplet state because of the different molecular packing. These self-consistent effects play a major role in the phosphorescence of crystals made of polar and polarizable molecular units, offering a powerful handle to tune the luminescence wavelength in the solid state through supramolecular engineering.

Emergent chiroptical properties in supramolecular and plasmonic assemblies.

This tutorial provides a comprehensive description of the origin of chiroptical properties of supramolecular and plasmonic assemblies in the UV-visible region of the electromagnetic spectrum. The photophysical concepts essential for understanding chiroptical signatures are presented in the first section. Just as the oscillator strength (a positive quantity) is related to absorption, the rotational strength (either a positive or a negative quantity) defines the emergence of chiroptical signatures in molecular/plasmonic systems.

Aggregates of polar dyes: beyond the exciton model.

The physics of aggregates of polar and polarizable donor-acceptor dyes is discussed, extending a previous model to account for the coupling of electronic and vibrational degrees of freedom. Fully exploiting translational symmetry, exact absorption and fluorescence spectra are calculated for aggregates with up to 6 molecules. A two-step procedure is presented: in the first step, a mean-field solution of the problem is proposed to define the excitonic basis via a rotation of the electronic basis.

Thermally activated delayed fluorescence: A critical assessment of environmental effects on the singlet-triplet energy gap.

The effective design of dyes optimized for thermally activated delayed fluorescence (TADF) requires the precise control of two tiny energies: the singlet-triplet gap, which has to be maintained within thermal energy, and the strength of spin-orbit coupling. A subtle interplay among low-energy excited states having dominant charge-transfer and local character then governs TADF efficiency, making models for environmental effects both crucial and challenging. The main message of this paper is a warning to the community of chemists, physicists, and material scientists working in the field: the adiabatic approximation implicitly imposed to the treatment of fast environmental degrees of freedom in quantum-classical and continuum solvation models leads to uncontrolled results.

Understanding TADF: a joint experimental and theoretical study of DMAC-TRZ.

Thermally-activated delayed fluorescence (TADF) is a promising strategy to harvest triplets in OLED towards improved efficiency, but several issues must be addressed to fully exploit its potential, including the nature of involved excited singlet and triplet states and their response to the local environment in order to concurrently optimize the dye inside the matrix. Towards this ambitious aim, we present an extensive spectroscopic study of a typical TADF dye in liquid and glassy solvents. TD-DFT results for the same molecule in gas-phase and under an applied electric field are exploited to build a reliable model for the dye, rigorously validated against experiment.

Understanding Förster Energy Transfer through the Lens of Molecular Dynamics.

A multiscale approach to the dynamics of resonant energy transfer (RET) is presented, combining DFT and TD-DFT results on the energy donor () and acceptor () moieties with an extensive equilibrium and non-equilibrium molecular dynamics (MD) analysis of a bound - pair in solution to build a coarse-grained kinetic model. We demonstrate that a thorough MD study is needed to properly address RET: the enormous configuration space visited by the system cannot be reliably sampled accounting only for a few representative configurations. Moreover, the conformational motion of the RET pair, occurring in a similar time scale as the RET process itself, leads to a sizable increase of the overall process efficiency.

Optical spectra of organic dyes in condensed phases: the role of the medium polarizability.

When designing molecular functional materials, the properties of the active specie, the dye, must be optimized fully accounting for the presence of a surrounding medium (a solvent, a polymeric matrix, etc.) that may largely alter the dye behavior. Here we present an effective model to account for the effects of the medium electronic polarizability on the spectral properties of charge-transfer dyes.

Supramolecular chirality: a caveat in assigning the handedness of chiral aggregates.

The handedness of a supramolecular chiral aggregate is often assigned based on the sign of circular dichroism spectra, adopting the exciton chirality method. However, the method does not properly account for the nature of intermolecular interactions. We introduce a generalized picture on the use of the sign of chiral signals in determining the helicity of chiral aggregates, rooted in the exciton model, supported by TD-DFT results.

Dye-Loaded Quatsomes Exhibiting FRET as Nanoprobes for Bioimaging.

Fluorescent organic nanoparticles (FONs) are emerging as an attractive alternative to the well-established fluorescent inorganic nanoparticles or small organic dyes. Their proper design allows one to obtain biocompatible probes with superior brightness and high photostability, although usually affected by low colloidal stability. Herein, we present a type of FONs with outstanding photophysical and physicochemical properties in-line with the stringent requirements for biomedical applications.

Antiadiabatic View of Fast Environmental Effects on Optical Spectra.

An antiadiabatic approach is proposed to model how the refractive index of the surrounding medium affects optical spectra of molecular systems in condensed phases. The approach solves some of the issues affecting current implementations of continuum solvation models and more generally of effective models where a classical description is adopted for the molecular environment.

About the origin of the large Stokes shift in aminoalkyl substituted heptamethine cyanine dyes.

Aminoalkyl-substituted heptamethine cyanine dyes are characterized by a large Stokes shift, an uncommon feature for cyanine molecules yet very promising for their application as fluorescent probes in bioimaging and as light harvesting antennas in biohybrid systems for solar energy conversion. The origin of this photophysical feature has not been adequately explored so far, and a combined experimental and theoretical work is herein provided to shed light on the role played by the central aminoalkyl substituent bound to the heptamethine cyanine backbone in defining the unusual properties of the dye. The spectra recorded in solvents of different polarities point to a marginal role of the medium in the definition of the Stokes shift, which conversely can be ascribed to the relaxation of the molecular geometry upon photoexcitation.

Addressing Charge-Transfer and Locally-Excited States in a Twisted Biphenyl Push-Pull Chromophore.

We present the synthesis and spectroscopic characterization of a twisted push-pull biphenyl molecule undergoing photoinduced electron transfer. Steady-state and transient absorption spectra suggest, in this rigid molecular structure, a subtle interplay between locally-excited and charge-transfer states, whose equilibrium and dynamics is only driven by solvation. A theoretical model is presented for the solvation dynamics and, with the support of quantum chemical calculations, we demonstrate the existence of two sets of states, having either local or charge-transfer character, that only "communicate" thanks to solvation, which is the sole driving force for the charge-separation process.

Excited-State Symmetry Breaking in an Aza-Nanographene Dye.

The photophysics of a structurally unique aza-analogue of polycyclic aromatic hydrocarbons characterized by 12 conjugated rings and a curved architecture was studied in detail. The combined experimental and computational investigation reveals that the lowest excited state has charge-transfer character, in spite of the absence of any peripheral electron-withdrawing groups. The exceptionally electron-rich core comprised of two fused pyrrole rings is responsible for it.

Chiral Plasmons: Au Nanoparticle Assemblies on Thermoresponsive Organic Templates.

Template-assisted strategies are widely used to fabricate nanostructured materials. By taking these strategies a step forward, herein we report the design of two chiral plasmonic nanostructures based on Au nanoparticle (NP) assemblies organized in clockwise and anticlockwise directions, having opposite response to circularly polarized light. The chiral plasmonic nanostructures are obtained by growing Au NPs on chiral templates based on d- and l-forms of alanine functionalized phenyleneethynylenes.

Intermolecular Energy Transfer in Real Time.

Resonance energy transfer (RET) is a complex phenomenon where energy is transferred between two nonequivalent molecules. In the Förster picture, that applies to the weak coupling regime, RET occurs from the energy donor molecule in the relaxed excited state toward the acceptor, in an energy-conserving process. However, energy dissipation is crucial for a more general picture of RET that also applies to the strong coupling regime.