ANDES, the high resolution spectrograph for the ELT: science case, baseline design and path to construction

Ground-based and airborne instrumentation for astronomy IX (2022), Montreal, JUL 17-22, 2022.--Proceedings of SPIE - The International Society for Optical Engineering vol. 12184 Article number 1218424.-- Complete list of authors: Marconi, A.; Abreu, M.; Adibekyan, V.; Alberti, V.; Albrecht, S.; Alcaniz, J.; Aliverti, M.; Allende Prieto, C.; Gomez, J. D. Alvarado; Amado, P. J.; Amate, M.; Andersen, M. I.; Artigau, E.; Baker, C.; Baldini, V.; Balestra, A.; Barnes, S. A.; Baron, F.; Barros, S. C. C.; Bauer, S. M.; Beaulieu, M.; Bellido-Tirado, O.; Benneke, B.; Bensby, T.; Bergin, E. A.; Biazzo, K.; Bik, A.; Birkby, J. L.; Blind, N.; Boisse, I.; Bolmont, E.; Bonaglia, M.; Bonfils, X.; Borsa, F.; Brandeker, A.; Brandner, W.; Broeg, C. H.; Brogi, M.; Brousseau, D.; Brucalassi, A.; Brynnel, J.; Buchhave, L. A.; Buscher, D. F.; Cabral, A.; Calderone, G.; Calvo-Ortega, R.; Cantalloube, F.; Canto Martins, B. L.; Carbonaro, L.; Chauvin, G.; Chazelas, B.; Cheffot, A. -L.; Cheng, Y. S.; Chiavassa, A.; Christensen, L.; Cirami, R.; Cook, N. J.; Cooke, R. J.; Coretti, I.; Covino, S.; Cowan, N.; Cresci, G.; Cristiani, S.; Cunha Parro, V.; Cupani, G.; D'Odorico, V.; de Castro Leao, I.; De Cia, A.; De Medeiros, J. R.; Debras, F.; Debus, M.; Demangeon, O.; Dessauges-Zavadsky, M.; Di Marcantonio, P.; Dionies, F.; Doyon, R.; Dunn, J.; Ehrenreich, D.; Faria, J. P.; Feruglio, C.; Fisher, M.; Fontana, A.; Fumagalli, M.; Fusco, T.; Fynbo, J.; Gabella, O.; Gaessler, W.; Gallo, E.; Gao, X.; Genolet, L.; Genoni, M.; Giacobbe, P.; Giro, E.; Goncalves, R. S.; Gonzalez, O. A.; Gonzalez Hernandez, J. I.; Gracia Temich, F.; Haehnelt, M. G.; Haniff, C.; Hatzes, A.; Helled, R.; Hoeijmakers, H. J.; Huke, P.; Jaervinen, A. S.; Jaervinen, S. P.; Kaminski, A.; Korn, A. J.; Kouach, D.; Kowzan, G.; Kreidberg, L.; Landoni, M.; Lanotte, A.; Lavail, A.; Li, J.; Liske, J.; Lovis, C.; Lucatello, S.; Lunney, D.; MacIntosh, M. J.; Madhusudhan, N.; Magrini, L.; Maiolino, R.; Malo, L.; Man, A. W. S.; Marquart, T.; Marques, E. L.; Martins, C. J. A. P.; Martins, A. M.; Maslowski, P.; Mason, E.; Mason, C. A.; McCracken, R. A.; Mergo, P.; Micela, G.; Mitchell, T.; Molliere, P.; Monteiro, M. A.; Montgomery, D.; Mordasini, C.; Morin, J.; Mucciarelli, A.; Murphy, M. T.; N'Diaye, M.; Neichel, B.; Niedzielski, A. T.; Niemczura, E.; Nortmann, L.; Noterdaeme, P.; Nunes, N. J.; Oggioni, L.; Oliva, E.; Onel, H.; Origlia, L.; Ostlin, G.; Palle, E.; Papaderos, P.; Pariani, G.; Penate Castro, J.; Pepe, F.; Levasseur, L. Perreault; Petit, P.; Pino, L.; Piqueras, J.; Pollo, A.; Poppenhaeger, K.; Quirrenbach, A.; Rauscher, E.; Rebolo, R.; Redaelli, E. M. A.; Reffert, S.; Reid, D. T.; Reiners, A.; Richter, P.; Riva, M.; Rivoire, S.; Rodriguez-Lopez, C.; Roederer, I. U.; Romano, D.; Rousseau, S.; Rowe, J.; Salvadori, S.; Sanna, N.; Santos, N. C.; Diaz, P. Santos; Sanz-Forcada, J.; Sarajlic, M.; Sauvage, J. -F.; Schaefer, S.; Schiavon, R. P.; Schmidt, T. M.; Selmi, C.; Sivanandam, S.; Sordet, M.; Sordo, R.; Sortino, F.; Sosnowska, D.; Sousa, S. G.; Stempels, E.; Strassmeier, K. G.; Suarez Mascareno, A.; Sulich, A.; Sun, X.; Tanvir, N. R.; Tenegi-Sangines, F.; Thibault, S.; Thompson, S. J.; Tozzi, A.; Turbet, M.; Vallee, P.; Varas, R.; Venn, K. A.; Veran, J. -P.; Verma, A.; Viel, M.; Wade, G.; Waring, C.; Weber, M.; Weder, J.; Wehbe, B.; Weingrill, J.; Woche, M.; Xompero, M.; Zackrisson, E.; Zanutta, A.; Zapatero Osorio, M. R.; Zechmeister, M.; Zimara, J.The first generation of ELT instruments includes an optical-infrared high resolution spectrograph, indicated as ELT-HIRES and recently christened ANDES (ArmazoNes high Dispersion Echelle Spectrograph). ANDES consists of three fibre-fed spectrographs (UBV, RIZ, YJH) providing a spectral resolution of similar to 100,000 with a minimum simultaneous wavelength coverage of 0.4-1.8 mu m with the goal of extending it to 0.35-2.4 mu m with the addition of a K band spectrograph. It operates both in seeing- and diffraction-limited conditions and the fibre-feeding allows several, interchangeable observing modes including a single conjugated adaptive optics module and a small diffraction-limited integral field unit in the NIR. Its modularity will ensure that ANDES can be placed entirely on the ELT Nasmyth platform, if enough mass and volume is available, or partly in the Coude room. ANDES has a wide range of groundbreaking science cases spanning nearly all areas of research in astrophysics and even fundamental physics. Among the top science cases there are the detection of biosignatures from exoplanet atmospheres, finding the fingerprints of the first generation of stars, tests on the stability of Nature's fundamental couplings, and the direct detection of the cosmic acceleration. The ANDES project is carried forward by a large international consortium, composed of 35 Institutes from 13 countries, forming a team of more than 200 scientists and engineers which represent the majority of the scientific and technical expertise in the field among ESO member states.The Italian effort for ANDES is supported by the Italian National Institute for Astrophysics (INAF). The Portuguese participation is supported by FCT -Fundacao para a Ciencia e a Tecnologia through national funds and by FEDER through COMPETE2020 -Programa Operacional Competitividade e Internacionalizacao by these grants: UID/FIS/04434/2019, UIDB/04434/2020 & UIDP/04434/2020; POCI-01-0145-FEDER-032113 & PTDC/FIS-AST/32113/2017. Swedish participation in the ANDES project is made possible through the national Swedish ELT Instrumentation Consortium (SELTIC), suppored by the Swedish Research Council (VR). CJM acknowledges FCT and POCH/FSE (EC) support through Investigador FCT Contract 2021.01214.CEECIND/CP1658/CT0001. JLB acknowledges funding from the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation program under grant agreement No 805445. MTM acknowledges the support of the Australian Research Council through Future Fellowship grant FT180100194 SS acknowledges funding from the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation program under grant agreement No 804240. TMS acknowledgment the support from the SNF synergia grant CRSII5-193689 (BLUVES)With funding from the Spanish government through the Severo Ochoa Centre of Excellence accreditation SEV-2017-0709Peer reviewe

Photochemical properties of Re(CO)3 complexes with and without a local proton source and implications for CO2 reduction catalysis

Herein, we present a detailed study on the photophysical properties and the excited state reactivity of two mononuclear Re(CO)3 complexes with imdazol-pyridine ligands equipped with and without a local proton source, [Re(CO)3LCl], where for 1: L = 2,4-ditert-butyl-6-(6-(1-methyl-1H-imidazol-2- yl)pyridin-2-yl)phenol and 2: L = 2-(3,5-ditert-butyl-2-methox-yphenyl)-6-(1-methyl-1H-imidazol-2-yl)pyridine. Time-resolved IR and UV/vis spectroscopy revealed that excitation of 1 and 2 is followed by population of the triplet excited state within <100 fs, where structural and vibrational relaxation to the T1 equilibrium structure is observed on the picosecond time scale. The T1 state can be viewed as a MLCT state as all ν(CO) features in the transient infrared (TRIR) spectra are shifted to higher wavenumbers upon excitation, which is indicative for a decreasing Re →COπ-backdonation. The T1 states have considerably long lifetimes at room temperature of 160 ns for 1 and 430 ns for 2 in dmf and they can be successfully quenched by the sacrificial electron donors triethanolamine (TEOA) and 1,3-dimethyl-2-phenyl-2,3-dihydro-1H-benzo[d]imidazole (BIH). The quenching rates are 2 orders of magnitude larger for BIH than for TEOA, as the latter reaction is endergonic. However, both species are not active in the photochemical CO2-to-CO conversion. We rationalize this for 2 by the low steady-state concentration of the initial reduction product, [Re(CO)3LCl]−, which ejects chloride rather fast. Thus, the second, homogeneous electron transfer process between [Re(CO)3LCl]− and [Re(CO)3L(solvent)] forming the active species [Re(CO)3L]−, has a very low probability and decomposition pathways come to the fore. 1 decomposes under irradiation in the presence of BIH or TEOA forming the initial photoproduct 3. We tentatively assume that the ligand in 3 is deprotonated and switches from a N,N- to a N,O−-coordination mode. This indicates that in the excited state the Re−N bond is cleaved quite easily, as this decomposition pathway has not been observed under electrochemical conditions

Time-resolved spectroscopy of photoinduced electron transfer in dinuclear and tetranuclear Fe/Co prussian blue analogues

The dynamics of the photodriven charge transfer- induced spin transition (CTIST) in two Fe/Co Prussian Blue Analogues (PBAs) are revealed by femtosecond IR and UV/vis pump−probe spectroscopy. Depending on temperature, the known tetranuclear square-type complex [Co 2 Fe 2 (CN) 6 (tp*) 2 (4,4′- dtbbpy) 4](PF 6)2 (1) exists in two electronic states. In acetonitrile solution, at 300 K. Photoexcitation into the intervalence charge transfer (IVCT) band of the LT phase at 800 nm induces electron transfer in one Fe−Co edge of PBA 1 and produces a [Fe IIILSCoIILS ] intermediate which by spin-crossover (SCO) is stabilized within 400 fs to a long-lived (>1 ns) [Fe IIILSCo IIHS] species. In contrast, IVCT excitation of the HT phase at 400 nm generates a [Fe IILSCoIIIHS] species with a lifetime of 3.6 ps. Subsequent back-electron transfer populates the vibrationally hot ground state, which thermalizes within 8 ps. The newly synthesized dinuclear PBA, [CoFe(CN)3(tp*)(pz*4Lut)]ClO 4 (2), provides a benchmark of the HT phase of 1, i.e., [Fe IIILSCo IIHS], as verified by variable temperature magnetic susceptibility measurements and 57 Fe Mö ssbauer spectroscopy. The photoinduced charge transfer dynamics of PBA 2 indeed are almost identical to that of the HT phase of PBA 1 with a lifetime of the excited [Fe IILSCoIIIHS ] species of 3.8 ps

Uniformity and wavefront control of optical filters

The present paper addresses uniformity effects in demanding dielectric optical coatings. The origins of spectral resonant wavefront errors (WFE) induced by non-uniformities in complex dielectric filters are investigated in detail. The coating is a broad-band beamsplitter with a high reflectance between 400 and 900 nm and a high transmittance between 920 and 2300nm. The WFE can significantly be reduced with an optimized design. A new setup based on Hartmann-Shack sensors measures the spectrally dependent WFE in the visual spectral range. The paper presents a method for referencing the measured data. The experimental WFE maps obtained by spectral Hartmann-Shack measurements agree well with the expected spectra taken from spectral photometric measurements and the coating design. The paper also addresses coatings on curved surfaces. A band pass filter centered at 670 nm on the convex side of a lens was developed. Using a combination of a sub-rotation and special uniformity masks, a very low spectral shift of the passband position overall the lens surface could be demonstrated. The deposition concept and mask design, respectively, are developed via simulation studies based on a simulation approach shown in [10]. Extension of the model framework by plasma simulation and a concept for computing deposition profiles on moving 3D substrates was required for solving the problem

Leishmania major Infection in Humanized Mice Induces Systemic Infection and Provokes a Nonprotective Human Immune Response

Background Leishmania (L.) species are the causative agent of leishmaniasis. Due to the lack of efficient vaccine candidates, drug therapies are the only option to deal with cutaneous leishmaniasis. Unfortunately, chemotherapeutic interventions show high toxicity in addition to an increased risk of dissemination of drug-resistant parasites. An appropriate laboratory animal based model is still missing which allows testing of new drug strategies in the context of human immune cells in vivo. Methodology/Principal Findings Humanized mice were infected subcutaneously with stationary phase promastigote L. major into the footpad. The human immune response against the pathogen and the parasite host interactions were analyzed. In addition we proved the versatility of this new model to conduct drug research studies by the inclusion of orally given Miltefosine. We show that inflammatory human macrophages get infected with Leishmania parasites at the site of infection. Furthermore, a Leishmania-specific human-derived T cell response is initiated. However, the human immune system is not able to prevent systemic infection. Thus, we treated the mice with Miltefosine to reduce the parasitic load. Notably, this chemotherapy resulted in a reduction of the parasite load in distinct organs. Comparable to some Miltefosine treated patients, humanized mice developed severe side effects, which are not detectable in the classical murine model of experimental leishmaniasis. Conclusions/Significance This study describes for the first time L. major infection in humanized mice, characterizes the disease development, the induction of human adaptive and innate immune response including cytokine production and the efficiency of Miltefosine treatment in these animals. In summary, humanized mice might be beneficial for future preclinical chemotherapeutic studies in systemic (visceral) leishmaniasis allowing the investigation of human immune response, side effects of the drug due to cytokine production of activated humane immune cells and the efficiency of the treatment to eliminate also not replicating (“hiding”) parasites

Exploring the light-induced dynamics in solvated metallogrid complexes with femtosecond pulses across the electromagnetic spectrum

Oligonuclear complexes of d4–d7 transition metal ion centers that undergo spin-switching have long been developed for their practical role in molecular electronics. Recently, they also have appeared as promising photochemical reactants demonstrating improved stability. However, the lack of knowledge about their photophysical properties in the solution phase compared to mononuclear complexes is currently hampering their inclusion into advanced light-driven reactions. In the present study, the ultrafast photoinduced dynamics in a solvated [2 × 2] iron(II) metallogrid complex are characterized by combining measurements with transient optical-infrared absorption and x-ray emission spectroscopy on the femtosecond time scale. The analysis is supported by density functional theory calculations. The photocycle can be described in terms of intra-site transitions, where the FeII centers in the low-spin state are independently photoexcited. The Franck–Condon state decays via the formation of a vibrationally hot high-spin (HS) state that displays coherent behavior within a few picoseconds and thermalizes within tens of picoseconds to yield a metastable HS state living for several hundreds of nanoseconds. Systematic comparison with the closely related mononuclear complex [Fe(terpy)2]2+ reveals that nuclearity has a profound impact on the photoinduced dynamics. More generally, this work provides guidelines for expanding the integration of oligonuclear complexes into new photoconversion schemes that may be triggered by ultrafast spin-switching