This band-like carrier conduction is beneficial in the development of high-performance organic field-effect transistors (OFETs). Among numerous layered OSCs developed thus far, unsymmetric rod-like organic molecules composed of π-electron cores linked with long alkyl chains (and/ or other substituents) have enabled the development of OSCs with excellent performance. The advantages of these materials are exemplified by the properties of substituted [1]benzothieno [3,2-b][1]benzothiophene (BTBT), [10][11][12][13][14] benzothieno [3,2b]naphtho [2,3-b]thiophene (BTNT), [15,16] and benzothieno-[6,5-b]benzothieno[3,2-b] thiophenes (BTBTTs). [17] Such molecules form unipolarly aligned monomolecular layers composed mostly of layeredherringbone (LHB) packing-an ideal form for 2D semiconducting carrier transport. In addition, each unipolar layer is stacked alternately to afford bilayer-type packing which we call bilayer-type LHB (b-LHB). [11,12,[18][19][20][21][22] A typical OSC is 2-alkyl-7-phenyl-where n represents the number of carbon atoms in the alkyl chain), which exhibits field-effect mobility greater than 10 cm 2 V −1 s −1 . [11,23] The b-LHB packing of Ph-BTBT-C n (n ≥ 5) is considerably stabilized by outer alkyl-chain layers, as demonstrated by intermolecular interaction calculations. [20,21] An intriguing feature is that the compound exhibits thermotropic liquid-crystalline (LC) transitions to smectic-E (SmE) and smectic-A (SmA) phases at elevated temperatures. [11] The large conformational degrees of freedom involved in the alkyl substituents might be associated with the emergence of LC phases. [24][25][26] Such alkylated OSCs also exhibit good solvent solubility, which is a critical feature for achieving availability in solution-based thin-film processing or printed electronics technologies. [27,28] On the basis of a molecular dynamics simulation, researchers found that the temporary LC-like layer formed at the liquid-air interface plays a critical role in the growth of a large-area and highly uniform selforganized OSC layer in solution processes. [29] However, the roles of the substituents and the process by which molecular ordering over LC states is controlled remain unclear.Recently, a substituent modification of Ph-BTBT-C n to 2-alkyl-7-phenylethynyl-BTBT (PE-BTBT-C n ), in which the phenyl group is substituted with an extended substituent of Organic semiconductors (OSCs) often exhibit thermotropic liquid-crystalline (LC) phases in which molecular orientational order is partially lost. The formation of a temporary LC state via a solution process is expected to promote printing-based device production, although a method of controlling molecular ordering over LC states has not yet been developed. Here, it is demonstrated that long-axis molecular ordering can be controlled under ambient conditions using unsymmetrically alkylated OSCs with high layered crystallinity. Introducing a small amount of OSC molecules with longer alkyl-chain lengths leads to the conversion of the long-axis disordered phase into a bila...