A METHOD FOR THE SYNTHESIS OF TRIS(ORTHO-CARBORANYL)BORANE BACKGROUND OF THE INVENTION Field of the Invention [01] Applicants’ invention relates to a method for synthesizing tris(ortho-carborane)borane (BoCb ₃ ). Applicants’ invention further relates to the resulting compound, tris(ortho- carborane)borane, which is an isolable, halide-free, single site, Lewis superacid. Background Information [02] Tris(pentafluorophenyl)borane (“BCF”) (see FIG.2a, B(C ₆ F ₅ ) ₃ ) was first reported in 1963. BCF and similar halide substituted Lewis acidic boranes (see FIGS. 2b, 2c [B(p-CF3-C6F4)3], 2d [Ar ^F = perfluoroaryl], and 2e [R ^F = CF3TeF3, SO2CF3]) are strong Lewis acids for promoting reactions. [03] A Lewis acid is a substance, such as an H ⁺ ion, that can accept a pair of nonbonding electrons, thus a Lewis acid is an electron-pair acceptor. Because it is a strong Lewis acid, it can be a co-catalyst for CH3- and H- abstraction, where abstraction is a chemical reaction in which there is the bimolecular removal of an atom from a molecular entity. CH3- requires a strong Lewis acid to be abstracted. [04] As a reagent, BCF can cause carbon-carbon bond formation. It can catalyze hydrogenation. It can cause a carbon ring to be opened or formed. It can cause bonds to be formed between a carbon molecule and another molecule. And it can cause silylation, which is the introduction of one or more silyl groups (Si R3) to a molecule. [05] Although BCF is a useful Lewis acid, it is not more Lewis acidic than the Lewis superacid, SbF5. [06] There are several boron based Lewis superacids that are known. Most of the methods to obtain them involve the slightest structural modifications of the BCF core, revolving around the fluorinated substituents. For instance, F atoms in BCF are replaced with CF ₃ , ammonium cations, or the fluorinated benzene core has been replaced with fluorinated naphthalene. Among many variants with differing fluoride substitution have been prepared but the only aryl substituted Lewis superacidic borane is B(p-CF3-C6F4)3 (see FIG.2c). Strong Lewis acidity has been achieved using rigid pyramidalized boranes tethered with carbon, phosphonium and sulfonium centers, although the free boranes are not isolable species and only found as a transient species or in solutions. [07] Boranes are useful Lewis acids in stoichiometric and catalytic reactions by taking advantage of the vacant p-orbital. Commonly found boron trihalides (BX ₃ ; X = F, Cl, Br) are example of this class; however, their volatile nature and the fragile B–X bonds make them incompatible with many substrates, thus limits its application. In this regard, the analogous tris(pentafluorophenyl)borane [B(C ₆ F ₅ ) ₃ ] commonly known as BCF (Figure 1), became the standout borane with excellent thermal stability and water and oxygen tolerant without compromising it’s Lewis acidity, which eventually established itself as a unique and powerful alternative and earned a recognized position in the borane-based Lewis acid catalysis. [08] Synthesis of tris(pentafluorophenyl)borane is a one-step process from commercially available reagents. It would be advantageous to increase the yield of the synthesis of tris(pentafluorophenyl)borane, which decreases costs as well as decreasing solvent and reagent waste. SUMMARY OF THE INVENTION [09] The present invention provides a novel process that will synthesize tris(ortho- carborane)borane (BoCb ₃ ). [10] BoCb3 is an isolable, halide-free, single site, Lewis superacid. The present invention involves the use of BoCb3 in promoting catalytic reactions. The compound, BoCb3, is disclosed for the first time. BoCb ₃ is a stronger Lewis acid than other stable boranes. [11] Traditionally, the three-coordinate boron motifs (BR3, R = aryl, alkyl, vinyl) are synthesized by reacting the corresponding organo-metal species (R-M, M = metal) with boron trihalides (BX3, X = Cl, Br). The lithiation of ortho-carborane with nBuLi and the subsequent reaction with 0.33 equivalents of BCl3 (1 M solution in hexanes) generates the desired BoCb3 generally 29% yield. Generally, “lithiation” involves a reaction with lithium or a lithium compound. Organolithium reagents are chemical compounds that contain carbon–lithium (C–Li) bonds. These reagents are frequently used to transfer the organic group or the lithium atom to a substrate. In this process, a boron trihalide is used for lithiating the ortho-carborane. When more electrophilic BBr3 is used instead of BCl3, the lithiated ortho-carborane produced a corresponding BoCb ₃ that achieved generally 35% isolated yields. [12] The geometry of BoCb3 is trigonal planar as all C–B–C bond angles are approximately 120º and the C-B bond lengths [1.614(8)-1.627(7) Å)] are slightly higher than the typical C(o- carborane)-B single bond in boranes species [1.58 Å]. [13] The downfield ¹¹ B{ ¹ H} resonance at 67.2 ppm is assigned to the central boron atom and peaks ranging from 7.4 to –12.4 ppm to the cluster atoms. The C–H protons are the most diagnostic in the ¹ H NMR spectrum and appear as a singlet at 5.02 ppm while the corresponding carbon is observed in the ¹³ C{ ¹ H} NMR spectrum at 65.0 ppm and a broad peak at 69.3 ppm is assigned to the ortho-carbons. The melting point is above 250 °C which indicates its thermal stability. BoCb3 is inert to oxygen. BoCb3 reacts slowly with water to give the free carborane and HOBoCb2. [14] Tris(ortho-carboranyl)borane shows reactivity with Lewis Bases and application in Frustrated Lewis Pair Si–H bond cleavage. Frustrated Lewis Pairs (“FLP”) arise from the combination of a Lewis acid and Lewis base that, due to steric demands, do not form a classical adduct. An “adduct” is a chemical species AB, where each molecular entity of which is formed by direct combination of two separate molecular entities A and B in such a way that there is change in connectivity, but no loss, of atoms within the moieties A and B. The reactivity of tris(ortho- carboranyl)borane with ubiquitous Lewis bases reveals only small Lewis bases bind. The tremendous bulk and Lewis acidity is leveraged in frustrated Lewis pair Si−H cleavage with a wider range of Lewis bases and greater efficacy than B(C6F5)3. [15] BoCb ₃ may be used for FLP chemistry using an alternative approach to fluorine loading of aryl groups to enhance Lewis acidity, ortho-carboranes as large electron withdrawing substituents. Tris(ortho-carboranyl)borane (BoCb3) is accessed in one pot from three commercially available chemicals. Mono- and bis-carboranylboranes have reported higher Lewis acidity than their aryl analogues but they are not as Lewis acidic as BoCb3. A competition experiment reacting an equimolar amount of acetonitrile with a fluoroarylborane B(C ₆ F ₅ ) ₃ and BoCb ₃ , indicates preferential binding to BoCb3. Calculated fluoride and hydride affinities, as well as ammonia and acetonitrile binding affinities, exceed the values reported for fluoroarylboranes. In addition to the greater Lewis acidity, the calculated steric profile of the fluoride adducts of BoCb ₃ revealed greater bulk at boron than B(C6F5)3 with a buried volume of 71.9% compared to 58.9%. It is anticipated that with the greater bulk of BoCb ₃ , a wider library of Lewis bases could be compatible for FLP chemistry. In the disclosure of BoCb3, acetonitrile (CH₃CN·BoCb3), triethylphosphine oxide (Et3PO·BoCb3), and benzaldehyde (PhC(H)O·BoCb3) adducts resulted. [16] It may be possible to produce FLPs with BoCb ₃ and a variety of commercially available Lewis bases. As examples, reacting BoCb3 with an equivalent of ethylacetate in CDCl3 results in the adduct (EtOAc·BoCb ₃ ) shows no change by ¹ H and ¹¹ B NMR spectroscopy, but the adduct can be crystallized in neat ethylacetate. Dissolving the crystals in CDCl3 revealed only free ethylacetate and BoCb3 indicating the adduct is not resilient in CDCl3 solution. [17] Reacting BoCb ₃ with 2,6-(CH ₃ ) ₂ C ₆ H ₃ NC generates the adduct, 2,6-(CH ₃ ) ₂ C ₆ H ₃ NC·BoCb ₃ . In this case, the adduct remains intact in CDCl3 solution as confirmed by ¹ H NMR spectroscopy with the three ortho C·H resonances shifted upfield (5.02 ppm to 4.7 2 ppm) along with the disappearance of the tricoordinate peak at 66.9 ppm in the ¹¹ B NMR spectrum. The corresponding ethylacetate and 2,6-(CH3)2C6H3NC adducts with B(C6F5)3 are resilient in solution. [18] The Lewis acidity of BoCb ₃ is higher than B(C ₆ F ₅ ) ₃ but only the ethylacetate adduct of BoCb3 dissociates in solution. The dissociation is likely occurs from the larger steric profile of BoCb ₃ versus B(C ₆ F ₅ ) ₃ . Therefore it is anticipated that BoCb ₃ is a good candidate as a Lewis acid for FLP chemistry. [19] The reactions of BoCb3 with an array of phosphines [PMe3, PPh3, PCy3, P(o-tol)3, P(p-Cl- C ₆ H ₄ ) ₃ , P(p-F-C ₆ H ₄ ) ₃ , and P(C ₆ F ₅ ) ₃ ] and amine bases (NEt ₃ and NPh ₃ ) in C ₆ D ₆ do not result in any adducts forming. B(C6F5)3 makes adducts with PMe3, PPh3, NEt3, PCy3, P(p-Cl-C6H4)3, and P(p- F-C ₆ H ₄ ) ₃ but not with P(o-tol) ₃ or P(C ₆ F ₅ ) ₃ . Thus, the breadth of Lewis bases for FLP generation with BoCb3 is much greater than B(C6F5)3. [20] BoCb3 is compatible with many Lewis bases to induce FLP Si–H cleavage. In the phosphine FLP systems, the stoichiometric reactions of BoCb ₃ and many phosphines (PR ₃ ; R = Me, Ph, Cy, p-Cl-C6H4) with HSiEt3 led to the ion pairs [R3PSiEt3][HBoCb3] in high yields while reactions with P(o-tol)3 and P(p-F-C6H4)3 required two equivalents of silane to consume the phosphine and BoCb ₃ starting materials. It is likely that the reduced reactivity of P(o-tol) ₃ is due to steric bulk, while P(p-F-C6H4)3 is from the lower Lewis basicity from the electron withdrawing fluorine. Further corroborating this, the fully fluorinated variant, P(C ₆ F ₅ ) ₃ , does not react with HSiEt3 in the presence of BoCb3, even with 5 equivalents of silane. The Tolman cone angles for P(o-tol)3 and P(C6F5)3 are similar (~184°) which implies that the electron withdrawing C6F5 group shuts down the reactivity. [21] The FLP reaction of BoCb3, NEt3, and HSiEt3 formed the [Et3NSiEt3][HBoCb3] ion pair but the reaction with NPh ₃ did not show any change in the ¹ H NMR and ¹¹ B NMR spectra. The diminished reactivity is rationalized by the weaker Lewis basicity of NPh3. Comparing the reactivity with the same phosphines and B(C ₆ F ₅ ) ₃ , the Ph ₃ P⋅B(C ₆ F ₅ ) ₃ adduct required 10 equivalents of HSiEt3 to achieve full conversion to the ion pair while (p-Cl-C6H4)3P⋅B(C6F5)3 and (p-F-C ₆ H ₄ ) ₃ P⋅B(C ₆ F ₅ ) ₃ resulted in only partial conversion with ten equivalents. The Cy3P⋅B(C6F5)3 adduct did not react with HSiEt3. [22] Solution NMR spectroscopy indicates that HSiEt ₃ interacts with B(C ₆ F ₅ ) ₃ , and heating to 60 °C leads to the formation of Piers’ borane, HB(C6F5)2. Contrarily, solution NMR spectroscopy does not reveal any interaction with BoCb ₃ , and heating to 120 °C did not result in any reaction. [23] A solution of [Ph3PSiEt3][HBoCb3] is stirred with an equivalent of B(C6F5)3 at 23 °C for an hour to determine whether B(C ₆ F ₅ ) ₃ or BoCb ₃ bind hydride more readily. There is no indication of hydride transfer from BoCb3 to B(C6F5)3 to form [HB(C6F5)3] based on ¹⁹ F{ ¹ H} and ¹ H NMR spectroscopy. The equimolar reaction of [NEt ₄ ][HB(C ₆ F ₅ ) ₃ ] and BoCb ₃ in CDCl ₃ at 23 °C resulted in partial conversion to [HBoCb3] and B(C6F5)3 based on ¹⁹ F{ ¹ H} and ¹ H NMR spectroscopy. Adding 1.4 equivalents of [NEt4][HB(C6F5)3] results in full conversion of BoCb3 to [NEt4][HBoCb3]. This is in line with the higher calculated hydride affinity of BoCb3 (622 kJ/mol cf. 484 kJ/mol). C ₆ D ₆ solution of BoCb ₃ and P ^t Bu ₃ or PMe ₃ solution to an atmosphere of CO ₂ at 23 °C did not result in any reaction by ¹ H and ¹¹ B NMR spectroscopy. Addition of HSiEt3 to attempt the hydrosilation of CO2 results in no reaction at 23 °C or at 80 °C. [24] Per the above, BoCb3 is resistant to forming adducts with a wide variety of bases but generates FLPs. The quenched reactivity could be applied to Si−H bond cleavage with triarylphosphines and trialkylphosphines to generate the phosphoniumsilane and tris- (orthocarboranyl)borohydride ion pairs, [R ₃ PSiEt ₃ ][HBoCb ₃ ]. In triarylphosphines, the bulk in P(o-tol)3 and electron withdrawing nature of P(p-F-C6H4)3 required an extra equivalent of silane. P(C ₆ F ₅ ) ₃ did not react at all. Notably, many of these do not react at all with B(C ₆ F ₅ ) ₃ and those that react require ten equivalents of triethylsilane. In regard to amines, NEt3 was effective but NPh3 did not induce any reactivity. The C–B–C bond angle in [HBoCb3] is more obtuse than in [HB(C ₆ F ₅ ) ₃ ], consistent with the steric profile. The greater hydride affinity of BoCb ₃ over B(C ₆ F ₅ ) ₃ was experimentally validated by competition studies with the respective hydride salts. These studies clearly indicate that BoCb ₃ is bulkier and has a higher hydride affinity than B(C ₆ F ₅ ) ₃ . This bodes well for FLP reactivity beyond Si–H cleavage. [25] It is also anticipated that BoCb3 would be useful as an olefin polymerization co-catalyst or activator. BoCb ₃ may also be useful as a Lewis acid catalyst for bond activation reactions to access useful chemicals from abundant feedstocks. BRIEF DESCRIPTION OF THE DRAWINGS [26] FIG. 1 illustrates the structure of BoCb ₃ . [27] FIGS. 2a-2e illustrates various, conventional forms of Lewis acids. [28] FIG. 3 illustrates the synthesis of BoCb3. [29] FIG. 4 is an expanded illustration of the synthesis of BoCb3. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT Ref. Element 10 Tris(ortho-carborane)borane (BoCb ₃ ) [30] Referring to the figures, FIG. 1 illustrates the solid state structure of tris(ortho- carborane)borane (BoCb3) 10, which is the compound that is the product of the described method of synthesis. [31] The ortho-carborane 12 has a chemical formula of oC ₂ B ₁₀ H ₁₂ . As shown in FIG. 1, the ortho-carborane structure 12 is generally a icosahedron (or 20-sided polyhedron) shaped structure, with the two (2) carbon molecules (14/16, 18/20, or 22/24) and the ten (10) boron atoms 28 at the vertices. In the figure, the hydrogen atoms (not shown) are omitted for clarity. The bonds 30 are represented by the lines between the vertices. [32] Each molecule of BoCb ₃ 10 has three (3) ortho-carborane structures 12. The ortho- carborane (oC2B10H12) 12 is abbreviated as oCb 12. Thus, the three (3) ortho-carboranes 12 are designated as the oCb ₃ portion in the BoCb ₃ . [33] The BoCb3 10 molecule is trigonal planar in shape or geometry. Trigonal refers to a geometrical arrangement of molecules having three branches connected to a central atom. Trigonal planar refers to the geometry where the three branches and the central atom are in the same general plane, as illustrated in FIG. 1. In BoCb3, the borane (B) 26 is the central atom, and the three (3) ortho-carboranes (oCb ₃ ) 12 are at the ends of the three (3) branches in the trigonal geometry. [34] One (1) of the primary carbon molecules (C(1) 14, C(2) 18, and C(3) 22) are bound to the central Boron atom 26, one in each of the three (3) ortho-carborane structures 12. The other substituent carbon molecules (16, 20, 24) are located in each of the three (3) ortho-carborane structures 12, and are bound in the ortho-carborane structure 12 at a vertex adjacent to that ortho- carborane structure’s 12 primary carbon molecules (14, 18, 22), which are, in turn, bound to the central Boron atom 26. The ortho (o) describes a molecule with substituents at adjacent positions in the structure, thus the ortho-carborane structures 12 have, for example, substituent carbon C(1)’ 16 adjacent or next to the primary carbon C(1) 14 on the icosahedron. The primary carbon C(1) 14 is bound to the central Boron (B) atom 26, carbon C(1)’ 16, and four (4) Boron atoms 28 in the ortho-carborane structure 12. [35] In the nitrile and isonitrile adducts, the CN bond lengths range from 1.1380 to 1.1448 Å, respectively. The FT-IR spectra showed the CN stretching frequency of CH ₃ CN·BoCb ₃ (2363 cm- ¹ ) is blue shifted in comparison to the (C6F5)3B·NCCH3 (2341 cm ^-1 ). Both metrics indicate a stronger CN bond upon coordination to BoCb ₃ 10 which signifies stronger coordination and a stronger Lewis acid. [36] In regard to the benzaldehyde adduct, the CO bond is 1.254 Å, and has a CO stretching frequency of PhC(H)O·BoCb ₃ (1584/1561 cm ^-1 ) is blue shifted from PhC(O)H·B(C ₆ F ₅ ) ₃ [1602 cm ^-1 ] which match the other results. In the ¹¹ B NMR spectra, the peak for the central boron atom (67.2 ppm) shifts to the tetracoordinate region among the cluster boron peaks. In the ¹ H NMR spectra, the C–H resonance of BoCb ₃ (5.02 ppm) in the ¹ H NMR spectrum shifts up-f d to 4.60, 4.77, and 4.72 ppm for CH3CN·BoCb3, PhC(O)H·BoCb3, and 2,6-(CH3)2C6H3NC·BoCb3, respectively. [37] The Gutmann-Beckett method was applied to evaluate the Lewis acidity of BoCb310. The Δδ ³¹ P value of BoCb310 is 31.9 ppm that is higher than the reported Lewis superacid B(p-CF3- C ₆ F ₄ ) ₃ , indicating BoCb ₃ 10 to be the stronger Lewis acid. [38] The very high experimental and theoretical Lewis acidity of BoCb3 10 indicates its potential as a catalyst in C–F bond activation reactions. There are only a few catalytic activities known with the boranes to activate the B-F bonds. It is noted that silanes do not seem to react with BoCb3 10 to form HBoCb2 or other unwanted side products. When 1 equivalent 1- fluoroadamantane is treated with 1 equivalent HSiEt ₃ in presence of 1 mol% BoCb ₃ in CDCl ₃ at room temperature for 10 minutes, it results in the reduction product adamantane in quantitative yield (89% isolated yield) along with FSiEt ₃ as side product. [39] When 1-fluoroadamantane is reacted with benzene in the presence of 5 mol% BoCb3, it resulted in the coupled product in 90% yield within 10 minutes. Lowering the catalyst loading to 1% does not affect the reaction outcome. Additionally, when B(C ₆ F ₅ ) ₃ and H ₂ O·B(C ₆ F ₅ ) ₃ are subjected to the same transformation, there is no, or negligible, product formation. However, increasing the catalyst loading of B(C ₆ F ₅ ) ₃ and H ₂ O·B(C ₆ F ₅ ) ₃ to 5 mol% resulted in the desired product in 14% yields. [40] FIGS. 2a-2e illustrates various, conventional forms of Lewis acids. [41] FIG. 3 illustrates the synthesis of BoCb310. Using an unconventional withdrawing group with significant steric protection results in the isolation of a new class of trigonal planar Lewis acids. Conventionally, carboranes offer both of these attributes. A Lewis acid, from the MO theory (MO theory is a theory designed to explain covalent bonding.) perspective, is a molecule that has a non-bonding lowest unoccupied molecular orbital (“LUMO”). The orbital needs to unoccupied, otherwise no electrons could be donated into it. For energy minimization arguments, electrons would be donated into the unoccupied orbital that has the lowest energy, which is the LUMO. [42] The steps of the method for synthesizing a volume of BoCb3 10 comprise starting with oCbH and treating it with 1.0 equivalent of nBuLi, C ₇ H ₈ at a temperature range of –78 °C to 23 °C for 10 hours or more, or a range of 10 hours to 24 hours, or in a preferred embodiment for generally 16 hours. The resultant is treated with 0.33 mol equivalent BX3 (where X is Cl or Br) at a temperature range of –78 °C to 23 °C , or 0 °C to 23 °C, for 4 days or more, or in a preferred embodiment for generally 7 days. The final product is BoCb3. When BCl3 is used, the isolated yield of BoCb ₃ is generally 29%. When more electrophilic BBr ₃ is used instead of BCl ₃ , the isolated yield of BoCb3 is generally 35%. [43] In contrast to fluoroaryl boranes, the carborane cluster is not expected delocalize the LUMO, primarily a p-orbital on boron. The icosahedral C ₂ B ₁₀ cluster is exceptionally stable and can act as a sigma withdrawing group if C-bound. The three-dimensional icosahedron presents a sphere-like steric profile to protect its center. Within the C ₂ B ₁₀ carboranes, three isomers exist with each classified based on the relative positioning of the carbon atoms, ortho (adjacent), meta (one boron between), and para in which the carbon atoms are on opposite sides of the icosahedron. Among these, the ortho isomer is the most electron withdrawing. [44] FIG. 4 is an expanded illustration of the synthesis of BoCb310. [45] To a stirred toluene (20 mL) solution of o-carborane (10.00 mol, 1.442 g) in a container such as a Schlenk flask at –780 ºC, nBuLi (10.00 mmol, 4.00 mL) is slowly added under nitrogen. After stirring the reaction mixture for an additional 16 hours at room temperature, BBr3 (3.333 mmol, 316.3 µL) in toluene (10 mL) is slowly added via a syringe at approximately –78 ºC, accomplished over a period of approximately 10 minutes. The reaction mixture is stirred for 4 days or more, or preferably approximately 7 days at room temperature. [46] After confirming completion of the reaction (monitored by ¹ H and ¹¹ B NMR spectroscopy), an additional 50 mL of toluene is added and the mixture filtered through a small pad of celite, which is washed with dichloromethane (3 × 10 mL). The solids are then removed from the combined filtrate under vacuum and 10 mL of diethyl ether is added to the solids to form a suspension, which is filtered through a glass frit and the white residue is washed with diethyl ether (2 × 5 mL). [47] The residue is dried under vacuum to get pure BoCb310 as a white solid. Single crystals for X-ray diffraction studies are grown from a 1:1 dichloromethane/chloroform solution of BoCb ₃ 10 by vapor diffusion into toluene. [48] Yield: 35%, 511 mg; mp: >260 °C; ¹ H NMR (400 MHz, CDCl3): δ = 5.02 (s, 3H), 1.11- 3.78 (m, 33H) ppm; ¹³ C{ ¹ H} NMR (101 MHz, CDCl ₃ ): δ = 69.3, 65.0 ppm; ¹³ C NMR (101 MHz, CDCl3): δ = 69.2, 6 5.0 (d, J = 190.0 Hz) ppm; ¹¹ B{ ¹ H} NMR (128 MHz, CDCl3): δ = 66.9 (s), 7.4 (s), –2.7 (s), –6.2 (s), –8.7 (s), –12.4 (s) ppm; ¹¹ B NMR: δ = 66.9 (s), 7.4 (d, J = 148.6 Hz), –2.7 (d, J = 152.4 Hz), –6.2 (d, J = 153.0 Hz), –8.6 (d, J = 156.5 Hz), –12.4 (d, J = 123.8 Hz) ppm; FT- IR (ranked intensity, cm ^–1 ): 3148 (4), 2575 (1), 1191 (12), 1105 (2), 1061 (6), 1031 (15), 982 (11), 936 (7), 788 (5), 726 (3), 696 (14), 663 (9), 594 (8), 516 (10), 465 (13); HRMS(–ESI): calcd 441.5762 for C6H34B31 [M+H] ^– found 441.5769; Elemental analysis: calcd C 16.36, H 7.55 for C6H33B31; found: C 16.17, H 7.71. [49] Unless otherwise specifically noted, the elements and articles depicted in the drawings are not necessarily drawn to scale, but they are illustrative of the described implementations and are intended to disclose the elements and articles illustrated as part of the specification, and the drawings further indicate relative size, angles, shapes, arrangement, placement, and like information to one of ordinary skill in the art regarding the elements and articles in the drawing. [50] Throughout this disclosure, a hyphenated form of a reference numeral refers to a specific instance of an element and the un-hyphenated form of the reference numeral refers to the element generically or collectively. Thus, for example, widget 12-1 would refer to a specific widget of a widget class 12, while the class of widgets may be referred to collectively as widgets 12 and any one of which may be referred to generically as a widget 12. [51] As used herein, “removably attached,” “removably attachable,” or “removable” mean that a first object that is coupled to a second object may be decoupled from the second object, or taken away from an attached position relative to the second object, using some force or movement. “Removably attached,” “removably attachable,” or “removable” further mean that if the first object is not coupled with the second object, the first object may be coupled to the second object or returned to the attached position, using some force or movement. Both the decoupling and the coupling may be accomplished without damaging either the first object or the second object. [52] When the terms “substantially,” “approximately,” “about,” or “generally” are used herein to modify a numeric value, range of numeric values, or list numeric values, the term modifies each of the numerals. Unless otherwise indicated, all numbers expressing quantities, units, percentages, and the like used in the present specification and associated claims are to be understood as being modified in all instances by the terms “approximately,” “about,” and “generally.” As used herein, the term “approximately” encompasses +/–5 of each numerical value. For example, if the numerical value is “approximately 80,” then it can be 80 +/–5, equivalent to 75 to 85. As used herein, the term “about” encompasses +/–10 of each numerical value. For example, if the numerical value is “about 80,” then it can be 80 +/–10, equivalent to 70 to 90. As used herein, the term “generally” encompasses +/–15 of each numerical value. For example, if the numerical value is “about 80,” then it can be 80% +/–15, equivalent to 65 to 95. Accordingly, unless indicated to the contrary, the numerical parameters (regardless of the units) set forth in the following specification and attached claims are approximations that may vary depending upon the desired properties sought to be obtained by the exemplary embodiments described herein. In some ranges, it is possible that some of the lower limits (as modified) may be greater than some of the upper limits (as modified), but one skilled in the art will recognize that the selected subset will require the selection of an upper limit in excess of the selected lower limit. [53] At the very least, and not limiting the application of the doctrine of equivalents to the scope of the claim, each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques. [54] The terms “inhibiting” or “reducing” or any variation of these terms refer to any measurable decrease, or complete inhibition, of a desired result. The terms “promote” or “increase” or any variation of these terms includes any measurable increase, or completion, of a desired result. [55] The term “effective,” as that term is used in the specification and/or claims, means adequate to accomplish a desired, expected, or intended result. [56] The terms “a” or “an” when used in conjunction with the term “comprising” in the claims and/or the specification may mean “one,” but it is also consistent with the meaning of “one or more,” “at least one,” and “one or more than one.” [57] The term “each” refers to each member of a set, or each member of a subset of a set. [58] The terms “comprising” (and any form of comprising, such as “comprise” and “comprises”), “having” (and any form of having, such as “have” and “has”), “including” (and any form of including, such as “includes” and “include”) or “containing” (and any form of containing, such as “contains” and “contain”) are inclusive or open-ended and do not exclude additional, unrecited elements or method steps. [59] In interpreting the claims appended hereto, it is not intended that any of the appended claims or claim elements invoke 35 U.S.C. 112(f) unless the words “means for” or “step for” are explicitly used in the particular claim. [60] It should be understood that, although exemplary embodiments are illustrated in the figures and description, the principles of the present disclosure may be implemented using any number of techniques, whether currently known or not. The present disclosure should in no way be limited to the exemplary implementations and techniques illustrated in the drawings and description herein. Thus, although the invention has been described with reference to specific embodiments, this description is not meant to be construed in a limited sense. Various embodiments may include some, none, or all of the enumerated advantages. Various modifications of the disclosed embodiments, as well as alternative embodiments of the inventions will become apparent to persons skilled in the art upon the reference to the description of the invention. It is, therefore, contemplated that the appended claims will cover such modifications that fall within the scope of the invention. Modifications, additions, or omissions may be made to the systems, apparatuses, and methods described herein without departing from the scope of the disclosure. For example, the operations of the systems and apparatuses disclosed herein may be performed by more, fewer, or other components in the methods described may include more, fewer, or other steps. Additionally, steps may be performed in any suitable order.