9 research outputs found
Synthesis, Characterization, and Thermodynamic Properties of the Rare Earth Coordination Complex [Sm(C<sub>6</sub>H<sub>4</sub>NO<sub>2</sub>)<sub>2</sub>·C<sub>9</sub>H<sub>6</sub>NO]
This article reports the synthesis and thermodynamic
properties
of a novel rare earth coordination complex, samarium chloride hexahydrate
(SmCl<sub>3</sub>·6H<sub>2</sub>O) with nicotinic acid (C<sub>6</sub>H<sub>5</sub>NO<sub>2</sub>) and 8-hydroxylquinoline (C<sub>9</sub>H<sub>7</sub>NO), whose composition and structure were characterized
by elemental analysis, molar conductance, thermogravimetric analysis
(TG–DTG), UV spectroscopy, IR spectroscopy, and X-ray powder
diffraction. During the process of coordination, C<sub>6</sub>H<sub>5</sub>NO<sub>2</sub> was bidentate-coordinated with the rare earth
ion (Sm<sup>3+</sup>) through an acidic group that was formed by removing
the proton; the hydroxyl oxygen atom and heterocyclic nitrogen atom
of C<sub>9</sub>H<sub>6</sub>NO<sup>–</sup> formed a chelate
ring with Sm<sup>3+</sup> for coordination. The X-ray powder diffraction
pattern demonstrated that the crystal type of [SmÂ(C<sub>6</sub>H<sub>4</sub>NO<sub>2</sub>)<sub>2</sub>·C<sub>9</sub>H<sub>6</sub>NO] is similar to that of C<sub>5</sub>H<sub>11</sub>NO<sub>2</sub>, with the cell parameters <i>a</i> = 5.426 nm, <i>b</i> = 22.105 nm, and <i>c</i> = 5.277 nm. At a constant
temperature of 298.15 K, the dissolution enthalpies of the reactants
and products of the coordination reaction in the optimized calorimetric
solvent were determined with an advanced solution–reaction
isoperibol microcalorimeter. The standard molar enthalpy change of
the coordination reaction was determined to be Δ<sub>r</sub><i>H</i><sub>m</sub><sup>Θ</sup> = (167.49 ± 0.39) kJ·mol<sup>–1</sup>. The standard molar enthalpy of formation of the title complex,
[SmÂ(C<sub>6</sub>H<sub>4</sub>NO<sub>2</sub>)<sub>2</sub>·C<sub>9</sub>H<sub>6</sub>NO], was estimated to be Δ<sub>f</sub><i>H</i><sub>m</sub><sup>Θ</sup>[SmÂ(C<sub>6</sub>H<sub>4</sub>NO<sub>2</sub>)<sub>2</sub>·C<sub>9</sub>H<sub>6</sub>NO(s), 298.15 K] = −(1483.4 ± 2.4)
kJ·mol<sup>–1</sup>, from a combination of the experimental
values of enthalpies of dissolution and some other auxiliary thermodynamic
data through a designed thermochemical cycle based on a supposed chemical
reaction
Table_4_Nanopore long-read RNAseq reveals transcriptional variations in citrus species.xlsx
The number of studies on plant transcriptomes using ONT RNAseq technology is rapidly increasing in recent. It is a powerful method to decipher transcriptomic complexity, particularly alternative splicing (AS) event detection. Citrus plants are the most important widely grown fruit crops. Exploring different AS events in citrus contributes to transcriptome improvement and functional genome study. Here, we performed ONT RNAseq in 9 species (Atalantia buxifolia, Citrus clementina, C. grandis, C. ichangensis, C. reticulata, C. sinensis, Clausena lansium, Fortunella hindsii, and Poncirus trifoliata), accompanied with Illumina sequencing. Non-redundant full-length isoforms were identified between 41,957 and 76,974 per species. Systematic analysis including different types of isoforms, number of isoforms per gene locus, isoform distribution, ORFs and lncRNA prediction and functional annotation were performed mainly focused on novel isoforms, unraveling the capability of novel isoforms detection and characterization. For AS events prediction, A3, RI, and AF were overwhelming types across 9 species. We analyzed isoform similarity and evolutionary relationships in all species. We identified that multiple isoforms derived from orthologous single copy genes among different species were annotated as enzymes, nuclear-related proteins or receptors. Isoforms with extending sequences on 5’, 3’, or both compared with reference genome were filtered out to provide information for transcriptome improvement. Our results provide novel insight into comprehending complex transcriptomes in citrus and valuable information for further investigation on the function of genes with diverse isoforms.</p
DataSheet_1_Nanopore long-read RNAseq reveals transcriptional variations in citrus species.pdf
The number of studies on plant transcriptomes using ONT RNAseq technology is rapidly increasing in recent. It is a powerful method to decipher transcriptomic complexity, particularly alternative splicing (AS) event detection. Citrus plants are the most important widely grown fruit crops. Exploring different AS events in citrus contributes to transcriptome improvement and functional genome study. Here, we performed ONT RNAseq in 9 species (Atalantia buxifolia, Citrus clementina, C. grandis, C. ichangensis, C. reticulata, C. sinensis, Clausena lansium, Fortunella hindsii, and Poncirus trifoliata), accompanied with Illumina sequencing. Non-redundant full-length isoforms were identified between 41,957 and 76,974 per species. Systematic analysis including different types of isoforms, number of isoforms per gene locus, isoform distribution, ORFs and lncRNA prediction and functional annotation were performed mainly focused on novel isoforms, unraveling the capability of novel isoforms detection and characterization. For AS events prediction, A3, RI, and AF were overwhelming types across 9 species. We analyzed isoform similarity and evolutionary relationships in all species. We identified that multiple isoforms derived from orthologous single copy genes among different species were annotated as enzymes, nuclear-related proteins or receptors. Isoforms with extending sequences on 5’, 3’, or both compared with reference genome were filtered out to provide information for transcriptome improvement. Our results provide novel insight into comprehending complex transcriptomes in citrus and valuable information for further investigation on the function of genes with diverse isoforms.</p
Table_1_Nanopore long-read RNAseq reveals transcriptional variations in citrus species.xlsx
The number of studies on plant transcriptomes using ONT RNAseq technology is rapidly increasing in recent. It is a powerful method to decipher transcriptomic complexity, particularly alternative splicing (AS) event detection. Citrus plants are the most important widely grown fruit crops. Exploring different AS events in citrus contributes to transcriptome improvement and functional genome study. Here, we performed ONT RNAseq in 9 species (Atalantia buxifolia, Citrus clementina, C. grandis, C. ichangensis, C. reticulata, C. sinensis, Clausena lansium, Fortunella hindsii, and Poncirus trifoliata), accompanied with Illumina sequencing. Non-redundant full-length isoforms were identified between 41,957 and 76,974 per species. Systematic analysis including different types of isoforms, number of isoforms per gene locus, isoform distribution, ORFs and lncRNA prediction and functional annotation were performed mainly focused on novel isoforms, unraveling the capability of novel isoforms detection and characterization. For AS events prediction, A3, RI, and AF were overwhelming types across 9 species. We analyzed isoform similarity and evolutionary relationships in all species. We identified that multiple isoforms derived from orthologous single copy genes among different species were annotated as enzymes, nuclear-related proteins or receptors. Isoforms with extending sequences on 5’, 3’, or both compared with reference genome were filtered out to provide information for transcriptome improvement. Our results provide novel insight into comprehending complex transcriptomes in citrus and valuable information for further investigation on the function of genes with diverse isoforms.</p
Table_3_Nanopore long-read RNAseq reveals transcriptional variations in citrus species.xlsx
The number of studies on plant transcriptomes using ONT RNAseq technology is rapidly increasing in recent. It is a powerful method to decipher transcriptomic complexity, particularly alternative splicing (AS) event detection. Citrus plants are the most important widely grown fruit crops. Exploring different AS events in citrus contributes to transcriptome improvement and functional genome study. Here, we performed ONT RNAseq in 9 species (Atalantia buxifolia, Citrus clementina, C. grandis, C. ichangensis, C. reticulata, C. sinensis, Clausena lansium, Fortunella hindsii, and Poncirus trifoliata), accompanied with Illumina sequencing. Non-redundant full-length isoforms were identified between 41,957 and 76,974 per species. Systematic analysis including different types of isoforms, number of isoforms per gene locus, isoform distribution, ORFs and lncRNA prediction and functional annotation were performed mainly focused on novel isoforms, unraveling the capability of novel isoforms detection and characterization. For AS events prediction, A3, RI, and AF were overwhelming types across 9 species. We analyzed isoform similarity and evolutionary relationships in all species. We identified that multiple isoforms derived from orthologous single copy genes among different species were annotated as enzymes, nuclear-related proteins or receptors. Isoforms with extending sequences on 5’, 3’, or both compared with reference genome were filtered out to provide information for transcriptome improvement. Our results provide novel insight into comprehending complex transcriptomes in citrus and valuable information for further investigation on the function of genes with diverse isoforms.</p
Table_2_Nanopore long-read RNAseq reveals transcriptional variations in citrus species.xlsx
The number of studies on plant transcriptomes using ONT RNAseq technology is rapidly increasing in recent. It is a powerful method to decipher transcriptomic complexity, particularly alternative splicing (AS) event detection. Citrus plants are the most important widely grown fruit crops. Exploring different AS events in citrus contributes to transcriptome improvement and functional genome study. Here, we performed ONT RNAseq in 9 species (Atalantia buxifolia, Citrus clementina, C. grandis, C. ichangensis, C. reticulata, C. sinensis, Clausena lansium, Fortunella hindsii, and Poncirus trifoliata), accompanied with Illumina sequencing. Non-redundant full-length isoforms were identified between 41,957 and 76,974 per species. Systematic analysis including different types of isoforms, number of isoforms per gene locus, isoform distribution, ORFs and lncRNA prediction and functional annotation were performed mainly focused on novel isoforms, unraveling the capability of novel isoforms detection and characterization. For AS events prediction, A3, RI, and AF were overwhelming types across 9 species. We analyzed isoform similarity and evolutionary relationships in all species. We identified that multiple isoforms derived from orthologous single copy genes among different species were annotated as enzymes, nuclear-related proteins or receptors. Isoforms with extending sequences on 5’, 3’, or both compared with reference genome were filtered out to provide information for transcriptome improvement. Our results provide novel insight into comprehending complex transcriptomes in citrus and valuable information for further investigation on the function of genes with diverse isoforms.</p
Table_5_Nanopore long-read RNAseq reveals transcriptional variations in citrus species.xlsx
The number of studies on plant transcriptomes using ONT RNAseq technology is rapidly increasing in recent. It is a powerful method to decipher transcriptomic complexity, particularly alternative splicing (AS) event detection. Citrus plants are the most important widely grown fruit crops. Exploring different AS events in citrus contributes to transcriptome improvement and functional genome study. Here, we performed ONT RNAseq in 9 species (Atalantia buxifolia, Citrus clementina, C. grandis, C. ichangensis, C. reticulata, C. sinensis, Clausena lansium, Fortunella hindsii, and Poncirus trifoliata), accompanied with Illumina sequencing. Non-redundant full-length isoforms were identified between 41,957 and 76,974 per species. Systematic analysis including different types of isoforms, number of isoforms per gene locus, isoform distribution, ORFs and lncRNA prediction and functional annotation were performed mainly focused on novel isoforms, unraveling the capability of novel isoforms detection and characterization. For AS events prediction, A3, RI, and AF were overwhelming types across 9 species. We analyzed isoform similarity and evolutionary relationships in all species. We identified that multiple isoforms derived from orthologous single copy genes among different species were annotated as enzymes, nuclear-related proteins or receptors. Isoforms with extending sequences on 5’, 3’, or both compared with reference genome were filtered out to provide information for transcriptome improvement. Our results provide novel insight into comprehending complex transcriptomes in citrus and valuable information for further investigation on the function of genes with diverse isoforms.</p
Metal–Organic Rotaxane Frameworks Assembly by Cucurbit[6]uril-Based Pseudorotaxanes and Mixed Ligands
Four
novel high-dimensional metal–organic rotaxane frameworks (MORFs)
were successfully fabricated by cucurbit[6]Âuril-based pseudorotaxanes
([PR43]) and rigid carboxylate ligands by adjusting the synthesis
temperature and the length of ligands. Compound <b>1</b> represents
a three periodic 2-fold interpenetrating dia network based on a binuclear
{Cd<sub>2</sub>Cl<sub>4</sub>O<sub>4</sub>} second building unit (SBU). <b>2</b> and <b>3</b> are isostructural pcu networks constructed
by binuclear and trinuclear cadmium clusters, respectively, while
compound <b>4</b> is a two-dimensional layered network with
a large grid 44.3 × 19.8 Å<sup>2</sup>. Furthermore, their
fluorescent properties in different solvents are investigated
Metal–Organic Rotaxane Frameworks Assembly by Cucurbit[6]uril-Based Pseudorotaxanes and Mixed Ligands
Four
novel high-dimensional metal–organic rotaxane frameworks (MORFs)
were successfully fabricated by cucurbit[6]Âuril-based pseudorotaxanes
([PR43]) and rigid carboxylate ligands by adjusting the synthesis
temperature and the length of ligands. Compound <b>1</b> represents
a three periodic 2-fold interpenetrating dia network based on a binuclear
{Cd<sub>2</sub>Cl<sub>4</sub>O<sub>4</sub>} second building unit (SBU). <b>2</b> and <b>3</b> are isostructural pcu networks constructed
by binuclear and trinuclear cadmium clusters, respectively, while
compound <b>4</b> is a two-dimensional layered network with
a large grid 44.3 × 19.8 Å<sup>2</sup>. Furthermore, their
fluorescent properties in different solvents are investigated