Dissertations / Theses on the topic 'TetraNuc'

Le travail présenté dans ce manuscrit regroupe deux études de spectroscopie γ. La première concerne les isomères des noyaux de néodyme autour de N=82. Ces noyaux, lorsqu'ils sont étudiés par des modèles de type Cranked-Nilsson-Strutinsky, présentent des états énergétiquement favorisés. Ils sont autant de candidats pour la recherche d'isomères de spin. Expérimentalement, un certain nombre d'états isomériques ont déjà été observés dans les noyaux de 138,139,140Nd sur lesquels porte cette étude. Afin de mieux caractériser ces états, une expérience a été menée en août 2009 à Jyväskylä auprès de l'ensemble de détection JUROGAM-RITU-GREAT. La réaction de fusion-évaporation 48Ca + 76Zr 144Nd* réalisée avec une cible mince a permis de produire majoritairement les noyaux 139,140Nd. Les noyaux produits, transportés au plan focal par le spectromètre RITU, sont implantés et le rayonnement émis par la décroissance des isomères est ensuite recueilli par l'ensemble de détection GREAT. Nous développerons l'analyse complète de cette expérience et nous montrerons les résultats émergents. Nous avons, par exemple, pu montrer l'alimentation du niveau 20+ de 140Nd ainsi que le placement énergétique du niveau isomérique du noyau 139Nd. La deuxième partie de ce travail s'articule autour de la recherche de la symétrie tétraédrique dans le noyau 156Gd. Cela a consisté à la fois en un travail de spectroscopie γ des bandes de parité positive de ce noyau, laquelle a fait émerger un certain nombre de nouvelles transitions. Le deuxième volet de cette étude consistait à simuler dans l'environnement ROOT - GEANT4 le seuil d'observation des signaux faibles avec le détecteur de rayonnements γ de nouvelle génération AGATA

Des calculs théoriques utilisant la méthode de champ moyen ont suggérée l'existence des formes du noyau avec la symétrie tétraédrique et/ou octraédrique dans la région des terres rares au voisinage des noyaux 156Gd et 160Yb. Dans les noyaux avec une symétrie tétraédrique pure, des transitions intra-bande E2 à bas spin dans des bandes de parité négative disparaissent ou sont très faibles. Ce travail est dédié à une recherche expérimentale de la symétrie tétraédrique dans le noyau 156Gd. Une expérience a été faite à Jyväskylä avec le multi-détecteur JUROGAM, sur la réaction de fusion - évaporation 154Sm(, 2n)156Gd. L'analyse des données, a établi les rapports d'embranchement de deux bandes de parité négative et a permis, par distribution angulaire, de connaître la nature d'une nouvelle transition. Les rapports d'embranchement obtenus sont comparables avec ceux des expériences précédentes et quelques limites supérieures ont été déterminées. L'absence de transitions à bas spin (I$^{pi}<9$) dans la bande de parité négative à spin impair a été confirmée. Ces résultats ont renforcé l'hypothèse d'une symétrie tétraédrique dans le noyau 156Gd. La spectroscopie gamma est l'outil majeure utilisé dans ce travail. Les principes ainsi qu'une étude de simulation réaliste sont détaillés dans ce manuscrit. La simulation avec des événements réalistes a été faite pour comparer la fonction de réponse de deux types de multidétecteurs EUROBALL et AGATA. Les résultats montrent que sous certain conditions la phase démonstrateur d'AGATA peut être utilisée pour la recherche d'événements rares.

Des calculs théoriques utilisant la méthode de champ moyen ont suggérée l'existence des formes du noyau avec la symétrie tétraédrique et/ou octraédrique dans la région des terres rares au voisinage des noyaux 156Gd et 160Yb. Dans les noyaux avec une symétrie tétraédrique pure, des transitions intra-bande E2 à bas spin dans des bandes de parité négative disparaissent ou sont très faibles. Ce travail est dédié à une recherche expérimentale de la symétrie tétraédrique dans le noyau 156Gd. Une expérience a été faite à Jyväskylä avec le multi-détecteur JUROGAM, sur la réaction de fusion - évaporation 154Sm(, 2n)156Gd. L'analyse des données, a établi les rapports d'embranchement de deux bandes de parité négative et a permis, par distribution angulaire, de connaître la nature d'une nouvelle transition. Les rapports d'embranchement obtenus sont comparables avec ceux des expériences précédentes et quelques limites supérieures ont été déterminées. L'absence de transitions à bas spin (I$^{pi}<9$) dans la bande de parité négative à spin impair a été confirmée. Ces résultats ont renforcé l'hypothèse d'une symétrie tétraédrique dans le noyau 156Gd. La spectroscopie gamma est l'outil majeure utilisé dans ce travail. Les principes ainsi qu'une étude de simulation réaliste sont détaillés dans ce manuscrit. La simulation avec des événements réalistes a été faite pour comparer la fonction de réponse de deux types de multidétecteurs EUROBALL et AGATA. Les résultats montrent que sous certain conditions la phase démonstrateur d'AGATA peut être utilisée pour la recherche d'événements rares.

This Ph.D. thesis has been concerned with the reinvestigation and improvement of the intermolecular 1,3-dipolar cycloaddition strategy using isoxazoles, towards the 3-acyltetramic acids (3-acylpyrrrolidine-2,4-diones) and also the investigation and development of the corresponding intramolecular strategy. A second generation of the intermolecular route was developed previously within our group and we have synthesised a variety of pyrroloisoxazoles, the 'masked' tetramic acids. We have modified and improved both the isoxazole formations and the peptide coupling reactions; we have further developed the chain extension at the isoxazole C-5 (tetramic acid C-3) substituent, testing the aldol-type reaction with some aromatic aldehydes and extending it to aliphatic aldehydes. We have demonstrated the condensation method using a strong base and hydroxyl adducts were obtained. Dehydration has been undertaken to yield the alkenyl C-5 side-chain. Development of the desmethyllaccarin, a derivative of the natural product laccarin, has also been attempted via the intermolecular route. A potential intramolecular route has the reversed sequence from the intermolecular route, by using the N-acylation product produced from an amino acid for the formation of a nitrile oxide and hence our building block pyrroloisoxazole by intramolecular dipolar cycloaddition. We have generated a nitro ketoester compound from the amino acid and investigation on the synthesis of the pyrroloisoxazole has been undertaken.

Thesis (M.S.)--University of Tennessee Health Science Center, 2008.
Title from title page screen (viewed on February 27, 2009). Research advisor: Richard E. Lee, Ph.D. Document formatted into pages (viii, 40 p. : ill.). Vita. Abstract. Includes bibliographical references (p. 36-40).

This thesis is divided into two parts. Part 1 covers the biosynthesis of the fungal metabolite tenellin, and Part 2 the metabolism of β-aminoisobutyrate m Streptomyces sp. Tenellin is a yellow pigment of the fungus Beamaria bassiana. It is of mixed biosynthetic origin, being derived from a polyketide moiety and the amino acid L-phenylalanine. The timing of the C-methylations of the polyketide chain is discussed in Chapter 2, which describes attempts to incorporate deuterium labelled partially assembled putative intermediates into the polyketide. The biosynthesis of the pyridone ring of tenellin requkes the condensation of the polyketide moiety with a rearranged phenylpropanoid unit derived from phenylalanine. The nature of this intriguing intramolecular rearrangement is discussed in Chapters 3 and 4. A phenylalanine derived tetramic acid, proposed as an intermediate in the biosynthesis, has been synthesised, and used in biosynthetic investigations. The results of these investigations and the subsequent identification of tyrosine as a closer precursor to tenellin argue against its intermediacy. The failure of [2-(^13)C(^2)H(^15)N]-phenylalanine to become incorporated intact suggests a transamination process for phenylalanine / tyrosine prior to incorporation. Preliminary investigations suggest para-hydroxy phenyllactate may be die substrate for the rearranging enzyme and a more direct precursor to tenellin. β-Aminoisobutyrate, the end product of reductive thymine catabolism, contributes to both the propionate and butyrate pools in Streptomyces sp. The pathway of incorporation into the isobutyrate / butyrate pool has been investigated, and confirmed to be the reverse of that known to occur in L-valine metabolism. A mutant strain of Streptomyces avemitilis, unable to produce isobutyrate, was used due to low level incorporations into the branched-chain fatty acids. This work was carried out in collaboration with Dr. Hamish McArthur, Pfizer Central Research Division, Groton, USA, and Dr. Kevin Reynolds, Department of Pharmaceutical Science, University of Maryland.

Doctor of Philosophy (PhD)
This thesis describes synthetic studies towards the HIV-1 integrase inhibitory natural products lithospermic acid and integramycin, resulting in a formal total synthesis of the former. A modular, flexible and convergent synthetic strategy to lithospermic acid was devised. In this approach, a Sonogashira coupling was used to unite the C1–C7 and C20–C27 fragments that were subsequently manipulated to then participate in the key step of the synthesis, a palladium-mediated carbonylative annulation. Reduction of the benzofuran nucleus with magnesium in methanol then provided the desired dihydrobenzofuran core of lithospermic acid. Various protecting group strategies were investigated to complete this sequence in an efficient manner. Further synthetic manipulations afforded the complete C1–C9/C19–C27 fragment, which was united with the C10–C18 fragment to deliver the entire carbon skeleton of lithospermic acid. A two step deprotection sequence was undertaken, however, complications with the final deprotective step prevented definitive proof that the total synthesis of lithospermic acid had been achieved. An alternate protecting group strategy was sought, and a formal total synthesis of lithospermic acid was achieved by intercepting an advanced intermediate from a previous total synthesis. Several strategies for the enantioselective synthesis of the dihydrobenzofuran core of lithospermic acid were evaluated, however, none proved successful. A synthetic route towards the tetramic acid subunit of integramycin was also investigated. 3- Methoxymaleimide was constructed using known chemistry, and the regioselective reduction of this ring system was developed. Attempts to further functionalise this ring system were thwarted by difficulties associated with handling. The scope of the regioselective reduction was investigated on an array of N- substituted methoxymaleimides with the procedure found to be generally high yielding and highly regioselective.

4, 4'-Dihydroxybenzophenone-2, 4-dinitrophenylhydrazone (A-007) has recently completed a phase-I clinical trial, and objective responses were seen in advanced breast cancer, lung cancer, ovarian cancer, melanoma, skin cancer and non-Hodgkin's lymphoma. Despite the promising results in the clinical trials, the major disadvantage to using A-007 as a broad-scale therapeutic is its poor water solubility. To make use of this promising anticancer drug either orally or intravenously, the short-term obstacle must be to overcome the limited solubility of A-007 in water. There are several approaches to overcome this obstacle. The first approach is to make hydrolysable prodrugs of A-007. The second approach is to make an A-007 complex with a water soluble host, such as cyclodextrin. We used a combination of these two previously described methods, i.e. transforming A-007 into a more water soluble prodrugs and then further increasing the prodrug water solubility by making their cyclodextrin inclusion complexes. Our syntheses and spectroscopic explorations of A-007 prodrugs are presented in this dissertation. Tetramic acid (2, 4 pyrrolidine-2, 4-dione ring system) containing compounds have been found to display a remarkable diversity of biological activities and have attracted the interest of medicinal and synthetic chemists. Magnesidin (1-acetyl-3-octanoyl-5-ethylidene tetramic acid) has strong antimicrobial activity against bacteria that cause gingivitis and dental plaque. Current efforts toward the synthesis of Magnesidin are discussed along with the plans for the completion of synthesis.

Magnesidin is a magnesium chelate of the 3-hexanoyl and 3-octanoyl tetramic acid derivatives isolated from Psuedomonas magensiorubra. Its activity against grampositive bacteria was found to be a specific target for Gingivitis, a dental plaque.Although the synthesis of magnesidin has been reported earlier, it was not reproducible. The highly polar nature and it’s ability to exhibit tautomerization makes their chemical behavior complex and difficult to predict its structure. A variety of reactions and an in depth understanding of the chemical structure is necessary to attain the synthesis of these compounds. This dissertation focuses on addressing the attempts towards the synthesis of Magnesidin by identifying the important intermediates necessary for the synthesis as β- keto esters, α,β-unsaturated amino esters. The focus of the work has been addressed by developing a TAG molecule approach, which is similar to the concept of solid phase synthesis except for the fact that the TAG molecule can be identified under UV and also can be detected using various spectroscopic techniques. Microwave synthesis has been explored and applied in to the synthesis of benzyl mono and di bromination, 1,3- benzodioxoles have been established. The benzyl mono bromination is applied to synthesize the TAG molecule, which is then applied in developing a method of synthesis for β-keto esters. The azide approach was used to synthesize the α,β- unsaturated amides, which are another essential class of compounds in the synthesis of magnesidin.

This thesis describes the synthesis and biological evaluation of a library of compounds containing the tetramic acid core in search of novel antibacterial drug candidates. Chapter 1 discusses the need for new antibiotics due to the emergence of virulent bacterial strains resistant to clinically available drugs and the hiatus in the discovery of new replacement antibitoics that has become a global threat to human health. Different platforms for antibacterial drug discovery and the re-emergence of natural products-based approach that has gained importance in the quest for novel antibiotics are discussed. In this regard, the intrinsic antibacterial activity of natural products containing a tetramate core structure and the strategies developed to synthesise the core scaffold are described. Chapter 2 discusses the use of ʟ-serine and ʟ-cysteine in tetramic acid synthesis and the application of ʟ-cysteine-derived thiazolidine templates suitable for stereoselective ring closing reactions to obtain the tetramic acid core with scope for further functionalization. Chapters 3 and 4 describe a range of synthetic routes for appropriate substitutions of the tetramate core for compound library generation. Elaboration of the tetramate core via carboxamide tetramate synthesis, Suzuki-Miyaura cross-coupling reactions, glycosylations and their aglycone analogue synthesis, etherification, tetramate-pyroglutamate systems, Buchwald aminations/amidations, cycloadditions and β-lactam hybrids as possible chemical modifications of the tetramate core structure are discussed. Chapter 5 describes the antibacetiral activity and physicochemical properties of the library of compounds synthesised. A preliminary evaluation of their antibiotic activity was conducted against S. aureus and E. coli using the hole-plate method. MICs of the tetramates synthesised were determined against several Gram-negative strains; Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa and Gram-positive strains; MRSA, Enterococcus faecalis and Streptococcus pneumoniae, in whole-cell bioassays. Physicochemical properties of the compound library were analysed to map the chemical space occupied by tetramates with potent antibacterial activity. Enzyme inhibition studies were conducted to identify possible modes of action that contribute to whole-cell antibiotic activity and in this regard, the inhibition of enzymes S. aureus topoisomerase IV, S. aureus RNA polymerase, E. coli RNA polymerase, E. coli gyrase and M. tuberculosis gyrase are discussed. Since plasma protein binding of compounds is an important factor that determines the bioavailability of antibiotics and their clinical outcome, a study of the binding affinity of these drug candidates to Human Serum Albumin (HSA) by both whole-cell bioassay and NMR spectroscopy-based protein binding experiments are discussed. Finally, a brief note on the potential of tetramic acids to function as proteasome inhibitors in anticancer chemotherapy is included at the end of this chapter.

An understanding of the underlying mechanisms by which proteins engage and communicate within the complex cellular environment is critical to the elucidation of the molecular basis of disease states and the development of safer, more efficacious drug therapies. Diverse cellular functions, including replication, transcription, cell growth and intracellular signal transduction, are governed by extensive networks of protein-protein interactions (PPIs). Disruption of the finely-tuned cellular networks due to the formation of aberrant or unregulated PPIs is implicated in the development and progression of cancer. As a result, over the last decade, PPI modulation has developed as an attractive molecular target for novel cancer therapies and as a powerful research tool in chemical biology to provide insight into the cellular transformations involved in carcinogenesis. Chapter 1 provides a review of the physiological importance of PPIs and the role they play in the development and progression of cancer. A summary of the challenges associated with targeting PPIs is given, highlighting the changing perception regarding the drugabbility of PPIs and the technological and conceptual advances driving this transformation. A brief overview of the approaches used to identify PPI modulators links the reader to the appropriate chapter for further discussion and utilisation of a selection of these methods. Chapter 2 describes the application of a virtual screening approach to discover PPI modulators. In particular, the development of an in silico – in vitro screening method to identify modulators of the protein interactome of the AAA+ protein reptin. The synthesis and optimisation of two hit compounds is outlined, with a discussion of their predicted binding modes, mode of action, potential as chemical tools and lead molecules for an anti-cancer drug discovery programme. Chapter 3 highlights the potential to discover PPI modulators from Nature's rich source of structurally complex, bioactive molecules. A synthetic approach to a sub-family of tetramic acid natural products is outlined, involving the development of a short, asymmetric synthesis of unnatural 4,4-disubstituted glutamic acid derivatives. The first total syntheses of the potent siderophore harzianic acid and the PAC3 PPI inhibitor JBIR-22 are reported. In addition, the potential role of a Diels-Alderase enzyme in the biosynthesis of JBIR-22 and the development of a chiral catalysed intramolecular Diels-Alder of an advanced JBIR-22 intermediate is investigated. Chapter 4 discusses the use of structure based design techniques in the development of PPI modulators. The process involved in the design of two series of inhibitors of PICK PDZ domain mediated interactions is outlined. This leads to the development and optimisation of synthetic routes to both series of inhibitors, including the utilisation of a strategic sp3-sp2 cross coupling reaction. Finally, preliminary biological assessment of the inhibitors is reported. Chapter 5 gives a brief overview of high-throughput screening (HTS) methods used to identify PPI modulators. The utilisation of a forward chemical genetics screen to identify the p53 activator MJ05 is described. A racemic and asymmetric route to MJ05 is developed and biochemical analysis of the two enantiomers of MJ05 is reported including the investigation of MJ05 as an adjuvant therapy for the treatment of cancer. Chapter 6 provides a general overview of the outcome of the different approaches used in this research to discover PPI modulators. Particular emphasis is placed on the development of chemical tools for the elucidation and dissection of the physiological role of protein-protein interactions and the identification of novel drug targets, in addition to the identification of lead molecules for PPI drug development programmes.

Dans ce manuscrit, nous présentons un mise en place et calcul d'un observable physique dans le cadre de la Gravité Quantique à Boucles covariante, pour un processus physique mettant en jeu la gravité quantique de façon non-perturbatif. Nous considerons la transition d'une région de trou noir à une région de trou blanc, traitée comme une transition de géométrie assimilable à un effet de tunnel gravitationnel. L'observable physique est le temps caractéristique dans lequel ce processus se déroule.Nous commençons par une dérivation formelle de haut--en--bas, allant de l'action de Hilbert-Einstein au ansatz qui définit les amplitudes de l'approche covariante de la GQB. Nous prenons ensuite le chemin de bas--en--haut, aboutissant à l'image d'une intégrale de chemin du type somme-de-géométries qui émerge à la limite semi-classique, et discutons son lien étroite avec une intégrale de chemin basé sur l'action de Regge. En suite, nous expliquons comment construire des paquets d'ondes décrivant des géométries spatiales quantiques, plongées dans un espace-temps quantique de signature Lorentzienne.Nous montrons que lors de la mise en œuvre de ces outils, nous avons une estimation simple des amplitudes décrivant des transitions de géométrie de façon probabiliste. Nous construisons un mise en place basée sur l'espace-temps Haggard-Rovelli, où une approche d'intégrale de chemin peut être appliquée naturellement. Nous procédons à une dérivation d'une expression explicite, analytiquement bien--définie et finie, pour une amplitude de transition décrivant ce processus. Nous utilisons ensuite l'approximation semi-classique pour estimer le temps caractéristique du phénomène
In this manuscript we present a calculation from covariant Loop Quantum Gravity, of a physical observable in a non-perturbative quantum gravitational physical process. The process regards the transition of a trapped region to an anti--trapped region and is treated as a quantum geometry transition akin to gravitational tunneling. The physical observable is the characteristic timescale in which the process takes place. We start with a top--to--bottom formal derivation of the ansatz defining the amplitudes for covariant LQG, starting from the Hilbert-Einstein action. We then take the bottom--to--top path, starting from the EPRL ansatz, to the sum--over--geometries path integral emerging in the semi-classical limit, and discuss its close relation to the naive path integral over the Regge action. We proceed to the construction of wave--packets describing quantum spacelike three-geometries that include a notion of embedding in a Lorentzian spacetime. We derive a simple estimation for the amplitudes describing geometry transition and show that a probabilistic description for such phenomena emerges, with the probability of the phenomena to take place being in general non-vanishing.The Haggard-Rovelli spacetime, modelling the spacetime surrounding the geometry transition region for a black to white hole process, is formulated. We then use the semi--classical approximation to give a general estimation of amplitudes describing the process. We conclude that the transition is predicted to be allowed by LQG, with a crossing time that is linear in the mass. The probability for the process to take place is suppressed but non-zero

博士
國立中央大學
物理學系
102
Rapid cooling below the melting temperature can prevent liquids from crystallization. The dynamics of the quenched liquid is slow and heterogeneous. In the past decade, the origin of the slow and heterogeneous motion of the quenched liquid was studied by the molecular dynamics (MD) simulation or colloidal experiments. However, to prevent crystallization, some size inhomogeneity are commonly introduced into the system. Considering that the interaction of real liquid molecules are usually anisotropic, can the anisotropic interaction replace the size inhomogeneity to prevent crystallization is still an open and important issue. In this work, we study the phase behavior and the dynamics of 2D rodlike liquids in different transient and steady states through the Langevin dynamics simulation. An intermediate tetratic phase is identified between the isotropic liquid state and the crystal state under cooling. Although the potential energy of the phase is higher than that of the crystal, the stable local tetratic orders provide a high barrier to prevent crystallization. Similar to the typical supercooled liquid, the heterogeneous dynamics in the tetratic state is observed. Moreover, the translational and orientational diffusions in the system are decoupled but the correlation between displacement and orientation change shows the increased coupling. The conflict can be explained by the typical cooperative excitations of the system. At low temperature, the occurrence of the orientational hopping deteriorates the local structure and induces the surrounding translational hopping. It means that the orientational hopping cannot independently occur. On the contrary, the translational hopping can independently occur without inducing any orientation change. The unilateral coupling may be a building block to explain the similar behavior about the coupling and decoupling between translational and rotational dynamics in a supercooled liquid. Although the presence of the tetratic order of make the system different from the standard supercooled liquid, it is observed that shorten the rod length can suppress the formation of the tetratic order and still sufficiently prevent crystallization. The result suggests the importance of the anisotropic shape of particles to prevent crystallization.

In this thesis we have explored the no equilibrium phase behavior and dynamics of an agitated monolayer of macroscopic rod-like particles. The main objective of this thesis was to highlight the ways in which even the simplest nonequilibrium 2Dliquid-crystallinen system differs qualitatively from its thermal equilibrium counter part. One major finding of ours is the extreme sensitivity to shape in these nonequilibrium systems. In chapter 3 we saw that tapering the ends of the particles induced a change from 2–fold ordering to 4–fold ordering. As far as we know, this is the first experimental observation of ‘tetratic’ correlations in equilibrium or nonequilibrium settings. This shape dependence is also pronounced in the single particle dynamics where, in chapter 5, we saw that similar-shaped objects behave differently even if they have dissimilar aspect ratios. Another important finding of ours is that the density fluctuations in the nonequilibrium nematic are not merely larger than, but qualitatively different from, those seen in their equilibrium counterparts: the fluctuations of the population, in a region containing on average N particles, grow much faster than √N . Then on equilibrium nature of the systems we study is clearly visible even at the single-particle level where we observe violations of equipartition in all the particles we study. The anomalous fluctuations we observe can be under stood in the light of theories of flocking. We have motivated why our system can be thought of as a granular flock and in chapter 4 presented various quantitative observations that justify this claim: we see giant fluctuations that decay only logarithmically in time as predicted by a theory of active nematics. This supports the idea that granular systems can provide a faithful imitation of the collective dynamics of living flocks, thus offering an attractive and easily control able system on which to test the predictions of flocking theories. A part from being a table-top experiment, , our system has the two substantial advantages over living systems that there are no products of metabolism which need removing and that the population remains constant. Our work highlights the fact that the fascinating phenomena of flocking ,coherent motion and large-scale in homogeneity seen in living matter can be obtained in a system in which particles do not communicate except by contact, have no sensing mechanisms and are not influenced by the spatially-varying pressures and incentives of a biological environment. Directions to go from here are aplenty. There is a lot that needs to be done towards understanding the origins of the anomalous fluctuations: do they arise due to the coupling of mass currents to gradients in the nematic director field or is there some other mechanism at play? Though the observed motion of disclinations suggests the former, a thorough hand systematic study of defect behavior is lacking. How defects interact and whether there is any analogy to thermal-equilibrium defect-behavior is completely unexplored, theoretically and experimentally. Indeed, this would be of interest purely as a problem in nonequilibrium statistical mechanics independent of whether or not the system is described by theories of active nematics. A part from settling the important, fundamental issues regarding the giant fluctuations, one can explore the entire spectrum of rod-like particles and study its dynamics and phase behaviour. What happens to collections of javelins that are agitated in 2D geometries? Do they form steadily-moving flocks? What about the short cylinders? We have seen that in the dilute limit they behave in a polar fashion but at high area fractions they form a polar, 4–fold correlated states. At Intermediate densities will they form a polar phase? Why is it that the long cylinders do not show any polar dynamics? What factors govern whether a particle is polar or not? Can one engineer particles to efficiently translate random impulses in to directed motion? Thus, even the single particle dynamics offers many avenues for experimental exploration. However, there is also scope for theoretical work in this direction. A sound theoretical understanding of the individual particle’s behaviour will then pave the way for a microscopic theory for the collective granular-rod state.. This can then be compared to the active and flocking literature which his, largely, of a phenomenological nature as of now. In conclusion, we would like to say that our experiments have revealed many important and fascinating nonequilibrium phenomena. Our experiments demonstrate situations where ‘effective equilibrium’ approaches are in adequate. Such descriptions can accommodate neither the slow, giant, collective fluctuations we observe nor the non-equipartition at the single-particle level. Finally, as is often the case, our studies have thrown open many more questions than they have answered. We hope our experiments stimulate further studies and we believe that we are witnessing the birth of a new subfield at the crossroads of granular physics and the physics of flocks.